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Understanding Visual Field Defects

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Jasmine Nguyen
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0% found this document useful (0 votes)
21 views172 pages

Understanding Visual Field Defects

Uploaded by

Jasmine Nguyen
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PPTX, PDF, TXT or read online on Scribd

1

Visual Field Defects

? ?
Here is a representation of the VF for each eye. Which is OD, and which OS?
2

Visual Field Defects

OS OD
Here is a representation of the VF for each eye. Which is OD, and which OS?
Remember, VFs are not drawn as if the pt is looking at you; they’re drawn as
if you are the pt!
3

Visual Field Defects

? ?

? ? ? ?

? ?

OS OD
Measured in degrees from fixation, how far does the normal VF extend
superiorly, inferiorly, nasally and temporally?
4

Visual Field Defects

60o 60o

100o 60o 60o 100o

70o 70o

OS OD
Measured in degrees from fixation, how far does the normal VF extend
superiorly, inferiorly, nasally and temporally?
(Don’t get too fixated on these specific numbers--different sources will give
slightly different values.)
5

Visual Field Defects

? ?

OS OD
Measured in degrees from fixation, how much of the VF is assessed via the
automated perimetry machines found in most ophthalmology practices?
6

Visual Field Defects

24o 24o

OS OD
Measured in degrees from fixation, how much of the VF is assessed via the
automated perimetry machines found in most ophthalmology practices?
The central 24 degrees
7

Visual Field Defects

? ?

OS OD
How far in degrees from fixation is the blind spot?
8

Visual Field Defects

15o 15o

OS OD
How far in degrees from fixation is the blind spot?
About 15 (again, don’t get too hung up on that
specific number.)
9

Visual Field Defects

most anterior
Retina
location

Anatomic locations for


lesions producing VF defects
10

Visual Field Defects

Retina

Optic nerve
next location

Anatomic locations for


lesions producing VF defects
11

Visual Field Defects

Retina

Optic nerve

Anatomic locations for


lesions producing VF defects

Optic
next chiasm
location
12

Visual Field Defects

Retina

Optic nerve

Anatomic locations for


lesions producing VF defects

Optic chiasm

general term for all locations


posterior to the previous one
13

Visual Field Defects

Retina

Optic nerve

Anatomic locations for


lesions producing VF defects

Optic chiasm

Retrochiasmal
14

Visual Field Defects

Clinically obvious
two very general dz
Retina categories of retinal dz
Clinically subtle dz

Optic nerve

Optic chiasm

Retrochiasmal
15

Visual Field Defects

Clinically obvious dz
Retina Clinically subtle dz

Optic nerve

Optic chiasm

Retrochiasmal
16

Visual Field Defects

Clinically obvious dz
Retina Clinically subtle dz
What is meant by clinically obvious vs clinically subtle retinal dz?

Optic nerve

Optic chiasm

Retrochiasmal
17

Visual Field Defects

Clinically obvious dz
Retina Clinically subtle dz
What is meant by clinically obvious vs clinically subtle retinal dz?
In clinically obvious disease, the retina will appear abnormal on
Optic nerve DFE, whereas in clinically subtle disease it will look normal

Optic chiasm

Retrochiasmal
18

Visual Field Defects

Clinically obvious dz (eg…?)


Retina Clinically subtle dz
What is meant by clinically obvious vs clinically subtle retinal dz?
In clinically obvious disease, the retina will appear abnormal on
Optic nerve DFE, whereas in clinically subtle disease it will look normal

What is an example of…


…clinically obvious disease?

Optic chiasm

Retrochiasmal
19

Visual Field Defects

Clinically obvious dz (eg…RP)


Retina Clinically subtle dz
What is meant by clinically obvious vs clinically subtle retinal dz?
In clinically obvious disease, the retina will appear abnormal on
Optic nerve DFE, whereas in clinically subtle disease it will look normal

What is an example of…


…clinically obvious disease? ‘Typical’ retinitis pigmentosa

Optic chiasm

Retrochiasmal
20

Visual Field Defects

Clinically obvious dz (eg…RP)


Retina Clinically subtle dz (eg…?)
What is meant by clinically obvious vs clinically subtle retinal dz?
In clinically obvious disease, the retina will appear abnormal on
Optic nerve DFE, whereas in clinically subtle disease it will look normal

What is an example of…


…clinically obvious disease? ‘Typical’ retinitis pigmentosa
---clinically subtle disease?

Optic chiasm

Retrochiasmal
21

Visual Field Defects

Clinically obvious dz (eg…RP)


Retina Clinically subtle dz (eg…CAR)
What is meant by clinically obvious vs clinically subtle retinal dz?
In clinically obvious disease, the retina will appear abnormal on
Optic nerve DFE, whereas in clinically subtle disease it will look normal

What is an example of…


…clinically obvious disease? ‘Typical’ retinitis pigmentosa
---clinically subtle disease? Cancer-associated retinopathy

Optic chiasm

Retrochiasmal
22

Visual Field Defects

Clinically obvious dz
Retina Clinically subtle dz

Let’s take a brief aside to cover optic nerve fundamentals


Optic nerve before we address optic nerve VF defects

Optic chiasm

Retrochiasmal
23

Visual Field Defects


The optic nerves are composed of what?
24

Visual Field Defects


The optic nerves are composed of what?
The axons of retinal ganglion cells
25

Visual Field Defects


The optic nerves are composed of what?
The axons of retinal ganglion cells

How many fibers (axons) comprise an optic nerve?


26

Visual Field Defects


The optic nerves are composed of what?
The axons of retinal ganglion cells

How many fibers (axons) comprise an optic nerve? Glaucoma book: 1.2-1.5M
Neuro: 1-1.2M
Depends upon which book you ask, but the answer 1.2M works Fundamentals: “more than a million”
27

Visual Field Defects


The optic nerves are composed of what?
The axons of retinal ganglion cells

Do they synapse in the region of the optic nerve head?


28

Visual Field Defects


The optic nerves are composed of what?
The axons of retinal ganglion cells

Do they synapse in the region of the optic nerve head?


No
29

Visual Field Defects


The optic nerves are composed of what?
The axons of retinal ganglion cells

Do they synapse in the region of the optic nerve head?


No

Where will they synapse?


30

Visual Field Defects


The optic nerves are composed of what?
The axons of retinal ganglion cells

Do they synapse in the region of the optic nerve head?


No

Where will they synapse?


Most will synapse in the lateral geniculate nucleus (LGN)
31

Visual Field Defects


The optic nerves are composed of what?
The axons of retinal ganglion cells

Do they synapse in the region of the optic nerve head?


No

Where will they synapse?


Most will synapse in the lateral geniculate nucleus (LGN)

Most? Where will the others synapse, and what are they responsible for?
32

Visual Field Defects


The optic nerves are composed of what?
The axons of retinal ganglion cells

Do they synapse in the region of the optic nerve head?


No

Where will they synapse?


Most will synapse in the lateral geniculate nucleus (LGN)

Most? Where will the others synapse, and what are they responsible for?
Most of the others are involved in the pupillary light reflex; they peel off just prior to reaching the LGN,
heading instead to the pretectum of the dorsal midbrain to synapse in the pretectal nuclei
33

Visual Field Defects


The optic nerves are composed of what?
The axons of retinal ganglion cells

Do they synapse in the region of the optic nerve head?


No

Where will they synapse?


Most will synapse in the lateral geniculate nucleus (LGN)

Most? Where will the others synapse, and what are they responsible for?
Most of the others are involved in the pupillary light reflex; they peel off just prior to reaching the LGN,
heading instead to the pretectum of the dorsal midbrain to synapse in the pretectal nuclei

‘Most’? Where will the others synapse, and what are they responsible for?
34

Visual Field Defects


The optic nerves are composed of what?
The axons of retinal ganglion cells

Do they synapse in the region of the optic nerve head?


No

Where will they synapse?


Most will synapse in the lateral geniculate nucleus (LGN)

Most? Where will the others synapse, and what are they responsible for?
Most of the others are involved in the pupillary light reflex; they peel off just prior to reaching the LGN,
heading instead to the pretectum of the dorsal midbrain to synapse in the pretectal nuclei

‘Most’? Where will the others synapse, and what are they responsible for?
The hypothalamus, where they are involved in modulating circadian responses
35

Visual Field Defects


The optic nerves are composed of what?
The axons of retinal ganglion cells

Do they synapse in the region of the optic nerve head?


No

Where will they synapse?


Most will synapse in the lateral geniculate nucleus (LGN)
For a more in-depth look at the optic nerve, see slide-set FELT6
Most? Where will the others synapse, and what are they responsible for?
Most of the others are involved in the pupillary light reflex; they peel off just prior to reaching the LGN,
heading instead to the pretectum of the dorsal midbrain to synapse in the pretectal nuclei

‘Most’? Where will the others synapse, and what are they responsible for?
The hypothalamus, where they are involved in modulating circadian responses
36

Visual Field Defects

Clinically obvious dz
Retina Clinically subtle dz

Depressions
two general
Optic nerve categories of ON
VF defects
Scotomas

Optic chiasm

Retrochiasmal
37

Visual Field Defects

Clinically obvious dz
Retina Clinically subtle dz

Depressions
Optic nerve
Scotomas

Optic chiasm

Retrochiasmal
38

Visual Field Defects

Clinically obvious dz
Retina Clinically subtle dz
What’s the difference between a
depression and a scotoma?
Depressions
A depression is an inward shifting
Optic nerve of the outer limit of the visual field,
Scotomas whereas a scotoma is an area of
field loss surrounded on all sides by
areas of normal sensitivity.

Optic chiasm

Retrochiasmal
39

Visual Field Defects

Clinically obvious dz
Retina Clinically subtle dz
What’s the difference between a
depression and a scotoma?
Depressions
A depression is an inward shifting
Optic nerve of the outer limit of the visual field,
Scotomas whereas a scotoma is an area of
field loss surrounded on all sides by
areas of normal sensitivity.

Optic chiasm

Retrochiasmal
40

Visual Field Defects

Clinically obvious dz
Retina Clinically subtle dz
Nasal step
three specific
Depressions Altitudinal
depressions
Temporal wedge
Optic nerve
Scotomas

Optic chiasm

Retrochiasmal
41

Visual Field Defects

Clinically obvious dz
Retina Clinically subtle dz
Nasal step
Depressions Altitudinal
Temporal wedge
Optic nerve
Scotomas

Optic chiasm

Retrochiasmal
42

Visual Field Defects

Clinically obvious dz
Retina Clinically subtle dz
Nasal step
Depressions Altitudinal
Temporal wedge
Optic nerve
Scotomas
Superior nasal step

Optic chiasm

Inferior nasal step

Retrochiasmal
43

Visual Field Defects

Clinically obvious dz
Retina Clinically subtle dz
Nasal step
Depressions Altitudinal
Temporal wedge
Optic nerve
Scotomas
Superior altitudinal

Optic chiasm

Inferior altitudinal

Retrochiasmal
44

Visual Field Defects

Clinically obvious dz
Retina Clinically subtle dz
Nasal step
Depressions Altitudinal
Temporal wedge
Optic nerve
Scotomas

Optic chiasm

Retrochiasmal
45

Visual Field Defects

Clinically obvious dz
Retina Clinically subtle dz
Nasal step
Depressions Altitudinal
Temporal wedge
Optic nerve
Scotomas three specific
Central
scotomas
Ceco-central

Optic chiasm

Retrochiasmal
46

Visual Field Defects

Clinically obvious dz
Retina Clinically subtle dz
Nasal step
Depressions Altitudinal
Temporal wedge
Optic nerve Arcuate
Scotomas Central
Ceco-central

Optic chiasm

Retrochiasmal
47

Visual Field Defects

Clinically obvious dz
Retina Clinically subtle dz
Nasal step
Depressions Altitudinal
Temporal wedge
Optic nerve Arcuate
Scotomas Central
Ceco-central
Superior arcuate

Optic chiasm
Inferior arcuate

Retrochiasmal
48

Visual Field Defects

Clinically obvious dz
What’s the difference between a central and a
Retina Clinically subtle
ceco-central dz
scotoma?
A central scotoma involves only fixation, whereas…
Nasal step
a ceco-central scotoma
Depressions Altitudinalinvolves fixation and
extends all the way toTemporal
the blindwedge
spot.
Optic nerve Arcuate
Scotomas Central
Ceco-central

Optic chiasm

Retrochiasmal
49

Visual Field Defects

Clinically obvious dz
What’s the difference between a central and a
Retina Clinically subtle
ceco-central dz
scotoma?
A central scotoma involves only fixation, whereas…
Nasal step
a ceco-central scotoma
Depressions Altitudinalinvolves fixation and
extends all the way toTemporal
the blindwedge
spot.
Optic nerve Arcuate
Scotomas Central
Ceco-central

Optic chiasm

Retrochiasmal
50

Visual Field Defects

Clinically obvious dz
What’s the difference between a central and a
Retina Clinically subtle
ceco-central dz
scotoma?
A central scotoma involves only fixation, whereas…
Nasal step
a ceco-central scotoma
Depressions Altitudinalinvolves fixation and
extends all the way toTemporal
the blindwedge
spot
Optic nerve Arcuate
Scotomas Central
Ceco-central

Optic chiasm

Retrochiasmal
51

Visual Field Defects

Clinically obvious dz
What’s the difference between a central and a
Retina Clinically subtle
ceco-central dz
scotoma?
A central scotoma involves only fixation, whereas…
Nasal step
a ceco-central scotoma
Depressions Altitudinalinvolves fixation and
extends all the way toTemporal
the blindwedge
spot
Optic nerve Arcuate
Scotomas Central
Ceco-central

Optic chiasm

(Take note: Bilateral ceco-central scotomas


could be mistaken for bitemporal VF loss!)
Retrochiasmal
52

Visual Field Defects

Another way to think about theClinically


optic nerve is withdzrespect to its topography at
obvious
the optic nerve head. Specifically, the retinal nerve fibers composing the optic
Retina
nerve can be divided into threeClinically
groups: subtle dz

#1?
Optic nerve Arcuate fibers
#2?
#3?
Nasal fibers
head

Optic chiasm
1

Retrochiasmal
53

Visual Field Defects

Another way to think about theClinically


optic nerve is withdzrespect to its topography at
obvious
the optic nerve head. Specifically, the retinal nerve fibers composing the optic
Retina
nerve can be divided into threeClinically
groups: subtle dz

Papillomacular bundle
Optic nerve Arcuate fibers
#2?
#3?
Nasal fibers
head

Optic chiasm

Retrochiasmal
54

Visual Field Defects

Another way to think about theClinically


optic nerve is withdzrespect to its topography at
obvious
the optic nerve head. Specifically, the retinal nerve fibers composing the optic
Retina
nerve can be divided into threeClinically
groups: subtle dz

Papillomacular bundle
Optic nerve Arcuate fibers
#2?
#3?
Nasal fibers
head

Optic chiasm 2

Retrochiasmal
55

Visual Field Defects

Another way to think about theClinically


optic nerve is withdzrespect to its topography at
obvious
the optic nerve head. Specifically, the retinal nerve fibers composing the optic
Retina
nerve can be divided into threeClinically
groups: subtle dz

Papillomacular bundle
Optic nerve Arcuate fibers
#3?
Nasal fibers
head

Optic chiasm

Retrochiasmal
56

Visual Field Defects

Another way to think about theClinically


optic nerve is withdzrespect to its topography at
obvious
the optic nerve head. Specifically, the retinal nerve fibers composing the optic
Retina
nerve can be divided into threeClinically
groups: subtle dz

Papillomacular bundle
Optic nerve Arcuate fibers
#3?
Nasal fibers
head

Optic chiasm
3

Retrochiasmal
57

Visual Field Defects

Another way to think about theClinically


optic nerve is withdzrespect to its topography at
obvious
the optic nerve head. Specifically, the retinal nerve fibers composing the optic
Retina
nerve can be divided into threeClinically
groups: subtle dz

Papillomacular bundle
Optic nerve Arcuate fibers
Nasal radiating fibers
head

Optic chiasm

Retrochiasmal
58

Visual Field Defects

Another way to think about theClinically


optic nerve is withdzrespect to its topography at
obvious
the optic nerve head. Specifically, the retinal nerve fibers composing the optic
Retina
nerve can be divided into threeClinically
groups: subtle dz

Papillomacular bundle
Optic nerve Arcuate fibers
Nasal radiating fibers
head

Optic chiasm The basic topography


of the RNFL looks a
lot like a fish!

Retrochiasmal
59

Visual Field Defects

Clinically obvious dz
Retina
Which of these VF defects aresubtle
Clinically associated
dz with damage to each group?
Nasal step
Papillomacular bundle Altitudinal
Temporal wedge ?
Optic nerve Arcuate fibers Arcuate

head Nasal radiating fibers Central


Ceco-central ?

Optic chiasm

Retrochiasmal
60

Visual Field Defects

Clinically obvious dz
Retina
Which of these VF defects aresubtle
Clinically associated
dz with damage to each group?
Nasal step
Papillomacular bundle Altitudinal
Temporal wedge
Optic nerve Arcuate fibers Arcuate
Nasal radiating fibers
head Central
Ceco-central

Optic chiasm

Retrochiasmal
61

Visual Field Defects

Clinically obvious dz
Retina
Which of these VF defects aresubtle
Clinically associated
dz with damage to each group?
Nasal step
Papillomacular bundle Altitudinal
Temporal wedge
Optic nerve Arcuate fibers Arcuate
Nasal radiating fibers
head Central
Ceco-central

Optic chiasm
Which sorts of optic neuropathy are implicated if a P-M bundle VF defect is present?
Conditions involving compromised cellular metabolism: Think toxic/metabolic,
nutritional deficiencies, inherited mitochondrial dz, etc

Retrochiasmal
Why do conditions affecting metabolism preferentially affect the P-M bundle?
Because the P-M fibers are small, unmyelinated, and extremely active metabolically.
Taken together, these characteristics make them more vulnerable than the rest of
the optic nerve to factors that adversely impact metabolism.
62

Visual Field Defects

Clinically obvious dz
Retina
Which of these VF defects aresubtle
Clinically associated
dz with damage to each group?
Nasal step
Papillomacular bundle Altitudinal
Temporal wedge
Optic nerve Arcuate fibers Arcuate
Nasal radiating fibers
head Central
Ceco-central

Optic chiasm
Which sorts of optic neuropathy are implicated if a P-M bundle VF defect is present?
Conditions involving compromised cellular metabolism: Think toxic/metabolic,
nutritional deficiencies, inherited mitochondrial dz, etc

Retrochiasmal
Why do conditions affecting metabolism preferentially affect the P-M bundle?
Because the P-M fibers are small, unmyelinated, and extremely active metabolically.
Taken together, these characteristics make them more vulnerable than the rest of
the optic nerve to factors that adversely impact metabolism.
63

Visual Field Defects

Clinically obvious dz
Retina
Which of these VF defects aresubtle
Clinically associated
dz with damage to each group?
Nasal step
Papillomacular bundle Altitudinal
Temporal wedge
Optic nerve Arcuate fibers Arcuate
Nasal radiating fibers
head Central
Ceco-central

Optic chiasm
Which sorts of optic neuropathy are implicated if a P-M bundle VF defect is present?
Conditions involving compromised cellular metabolism: Think toxic/metabolic,
nutritional deficiencies, inherited mitochondrial dz, etc

Retrochiasmal
Why do conditions affecting metabolism preferentially affect the P-M bundle?
Because the P-M fibers are small, unmyelinated, and extremely active metabolically.
Taken together, these characteristics make them more vulnerable than the rest of
the optic nerve to factors that adversely impact metabolism.
64

Visual Field Defects

Clinically obvious dz
Retina
Which of these VF defects aresubtle
Clinically associated
dz with damage to each group?
Nasal step
Papillomacular bundle Altitudinal
Temporal wedge
Optic nerve Arcuate fibers Arcuate
Nasal radiating fibers
head Central
Ceco-central

Optic chiasm
Which sorts of optic neuropathy are implicated if a P-M bundle VF defect is present?
Conditions involving compromised cellular metabolism: Think toxic/metabolic,
nutritional deficiencies, inherited mitochondrial dz, etc

Retrochiasmal
Why do conditions affecting metabolism preferentially affect the P-M bundle?
Because the P-M fibers are small, unmyelinated, and extremely active metabolically.
Taken together, these characteristics make them more vulnerable than the rest of
the optic nerve to factors that adversely impact metabolism.
65

Visual Field Defects


Toxins that shouldn’t be ingested at all:
--
--
--
--(many others)
Clinically
Toxins that shouldn’t be ingested obvious
in large dz
quantities

Retina
for prolonged periods:
Which of these VF defects
--
aresubtle
Clinically associated
dz with damage to each group?
-- Nasal step
Toxins you were told to ingest by a doc:
--
Papillomacular bundle Altitudinal
Temporal wedge
Optic nerve
--
--
Arcuate fibers Arcuate
Nasal radiating fibers
head --
--
Central
Ceco-central
Nutrients that weren’t ingested in sufficient quantity:
--
--
--
Optic chiasm
Inherited mitochondrial diseases:
--
Which
-- sorts of optic neuropathy are implicated if a P-M bundle VF defect is present?
Conditions involving compromised cellular metabolism: Think toxic/metabolic,
nutritional deficiencies, inherited mitochondrial dz, etc

Retrochiasmal
Why do conditions affecting metabolism preferentially affect the P-M bundle?
Because the P-M fibers are small, unmyelinated, and extremely active metabolically.
Taken together, these characteristics make them more vulnerable than the rest of
the optic nerve to factors that adversely impact metabolism.
66

Visual Field Defects


Toxins that shouldn’t be ingested at all:
--Methanol
--Ethylene glycol
--Lead (in children)
--(many others)
Clinically
Toxins that shouldn’t be ingested obvious
in large dz
quantities

Retina
for prolonged periods:
Which of these VF defects
--
aresubtle
Clinically associated
dz with damage to each group?
-- Nasal step
Toxins you were told to ingest by a doc:
--
Papillomacular bundle Altitudinal
Temporal wedge
Optic nerve
--
--
Arcuate fibers Arcuate
Nasal radiating fibers
head --
--
Central
Ceco-central
Nutrients that weren’t ingested in sufficient quantity:
--
--
--
Optic chiasm
Inherited mitochondrial diseases:
--
Which
-- sorts of optic neuropathy are implicated if a P-M bundle VF defect is present?
Conditions involving compromised cellular metabolism: Think toxic/metabolic,
nutritional deficiencies, inherited mitochondrial dz, etc

Retrochiasmal
Why do conditions affecting metabolism preferentially affect the P-M bundle?
Because the P-M fibers are small, unmyelinated, and extremely active metabolically.
Taken together, these characteristics make them more vulnerable than the rest of
the optic nerve to factors that adversely impact metabolism.
67

Visual Field Defects


Toxins that shouldn’t be ingested at all:
--Methanol
--Ethylene glycol
--Lead (in children)
--(many others)
Clinically
Toxins that shouldn’t be ingested obvious
in large dz
quantities

Retina
for prolonged periods:
Which of these VF defects
--
aresubtle
Clinically associated
dz with damage to each group?
-- Nasal step
Toxins you were told to ingest by a doc:
--
Papillomacular bundle Altitudinal
Temporal wedge
Optic nerve
--
--
Arcuate fibers Arcuate
Nasal radiating fibers
head --
--
Central
Ceco-central
Nutrients that weren’t ingested in sufficient quantity:
--
--
--
Optic chiasm
Inherited mitochondrial diseases:
--
Which
-- sorts of optic neuropathy are implicated if a P-M bundle VF defect is present?
Conditions involving compromised cellular metabolism: Think toxic/metabolic,
nutritional deficiencies, inherited mitochondrial dz, etc

Retrochiasmal
Why do conditions affecting metabolism preferentially affect the P-M bundle?
Because the P-M fibers are small, unmyelinated, and extremely active metabolically.
Taken together, these characteristics make them more vulnerable than the rest of
the optic nerve to factors that adversely impact metabolism.
68

Visual Field Defects


Toxins that shouldn’t be ingested at all:
--Methanol
--Ethylene glycol
--Lead (in children)
--(many others)
Clinically
Toxins that shouldn’t be ingested obvious
in large dz
quantities

Retina
for prolonged periods:
Which of these VF defects
--Ethanol
aresubtle
Clinically associated
dz with damage to each group?
--Tobacco Nasal step
Toxins you were told to ingest by a doc:
--
Papillomacular bundle Altitudinal
Temporal wedge
Optic nerve
--
--
Arcuate fibers Arcuate
Nasal radiating fibers
head --
--
Central
Ceco-central
Nutrients that weren’t ingested in sufficient quantity:
--
--
--
Optic chiasm
Inherited mitochondrial diseases:
--
Which
-- sorts of optic neuropathy are implicated if a P-M bundle VF defect is present?
Conditions involving compromised cellular metabolism: Think toxic/metabolic,
nutritional deficiencies, inherited mitochondrial dz, etc

Retrochiasmal
Why do conditions affecting metabolism preferentially affect the P-M bundle?
Because the P-M fibers are small, unmyelinated, and extremely active metabolically.
Taken together, these characteristics make them more vulnerable than the rest of
the optic nerve to factors that adversely impact metabolism.
69

Visual Field Defects


Toxins that shouldn’t be ingested at all:
--Methanol
--Ethylene glycol
--Lead (in children)
--(many others)
Clinically
Toxins that shouldn’t be ingested obvious
in large dz
quantities

Retina
for prolonged periods:
Which of these VF defects
--Ethanol
aresubtle
Clinically associated
dz with damage to each group?
--Tobacco Nasal step
Toxins you were told to ingest by a doc:
--
Papillomacular bundle Altitudinal
Temporal wedge
Optic nerve
--
--
Arcuate fibers Arcuate
Nasal radiating fibers
head --
--(many others)
Central
Ceco-central
Nutrients that weren’t ingested in sufficient quantity:
--
--
--
Optic chiasm
Inherited mitochondrial diseases:
--
Which
-- sorts of optic neuropathy are implicated if a P-M bundle VF defect is present?
Conditions involving compromised cellular metabolism: Think toxic/metabolic,
nutritional deficiencies, inherited mitochondrial dz, etc

Retrochiasmal
Why do conditions affecting metabolism preferentially affect the P-M bundle?
Because the P-M fibers are small, unmyelinated, and extremely active metabolically.
Taken together, these characteristics make them more vulnerable than the rest of
the optic nerve to factors that adversely impact metabolism.
70

Visual Field Defects


Toxins that shouldn’t be ingested at all:
--Methanol
--Ethylene glycol
--Lead (in children)
--(many others)
Clinically
Toxins that shouldn’t be ingested obvious
in large dz
quantities

Retina
for prolonged periods:
Which of these VF defects
--Ethanol
aresubtle
Clinically associated
dz with damage to each group?
--Tobacco Nasal step
Toxins you were told to ingest by a doc:
--Amiodarone
Papillomacular bundle Altitudinal
Temporal wedge
Optic nerve
--Ethambutol
--Isoniazid
Arcuate fibers Arcuate
Nasal radiating fibers
head --Linezolid
--(many others)
Central
Ceco-central
Nutrients that weren’t ingested in sufficient quantity:
--
--
--
Optic chiasm
Inherited mitochondrial diseases:
--
Which
-- sorts of optic neuropathy are implicated if a P-M bundle VF defect is present?
Conditions involving compromised cellular metabolism: Think toxic/metabolic,
nutritional deficiencies, inherited mitochondrial dz, etc

Retrochiasmal
Why do conditions affecting metabolism preferentially affect the P-M bundle?
Because the P-M fibers are small, unmyelinated, and extremely active metabolically.
Taken together, these characteristics make them more vulnerable than the rest of
the optic nerve to factors that adversely impact metabolism.
71

Visual Field Defects


Toxins that shouldn’t be ingested at all:
--Methanol
--Ethylene glycol
--Lead (in children)
--(many others)
Clinically
Toxins that shouldn’t be ingested obvious
in large dz
quantities

Retina
for prolonged periods:
Which of these VF defects
--Ethanol Clinicallyaresubtle
associated
dz with damage to each group?
--Tobacco Nasal step
Toxins you were told to ingest by a doc:
--Amiodarone
Papillomacular bundle Altitudinal
Temporal wedge
Optic nerve
--Ethambutol
--Isoniazid
Arcuate fibers Arcuate
Nasal radiating fibers
head --Linezolid
--(many others)
Central
Ceco-central
Nutrients that weren’t ingested in sufficient quantity:
--
--
--
Optic chiasm
Inherited mitochondrial diseases:
--
Which
-- sorts of optic neuropathy are implicated if a P-M bundle VF defect is present?
Conditions involving compromised cellular metabolism: Think toxic/metabolic,
nutritional deficiencies, inherited mitochondrial dz, etc

Retrochiasmal
Why do conditions affecting metabolism preferentially affect the P-M bundle?
Because the P-M fibers are small, unmyelinated, and extremely active metabolically.
Taken together, these characteristics make them more vulnerable than the rest of
the optic nerve to factors that adversely impact metabolism.
72

Visual Field Defects


Toxins that shouldn’t be ingested at all:
--Methanol
--Ethylene glycol
--Lead (in children)
--(many others)
Clinically
Toxins that shouldn’t be ingested obvious
in large dz
quantities

Retina
for prolonged periods:
Which of these VF defects
--Ethanol Clinicallyaresubtle
associated
dz with damage to each group?
--Tobacco Nasal step
Toxins you were told to ingest by a doc:
--Amiodarone
Papillomacular bundle Altitudinal
Temporal wedge
Optic nerve
--Ethambutol
--Isoniazid
Arcuate fibers Arcuate
Nasal radiating fibers
head --Linezolid
--(many others)
Central
Ceco-central
Nutrients that weren’t ingested in sufficient quantity:
--Vitamin B12
--Folate

Optic chiasm
--Thiamine
Inherited mitochondrial diseases:
--
Which
-- sorts of optic neuropathy are implicated if a P-M bundle VF defect is present?
Conditions involving compromised cellular metabolism: Think toxic/metabolic,
nutritional deficiencies, inherited mitochondrial dz, etc

Retrochiasmal
Why do conditions affecting metabolism preferentially affect the P-M bundle?
Because the P-M fibers are small, unmyelinated, and extremely active metabolically.
Taken together, these characteristics make them more vulnerable than the rest of
the optic nerve to factors that adversely impact metabolism.
73

Visual Field Defects


Toxins that shouldn’t be ingested at all:
--Methanol
--Ethylene glycol
--Lead (in children)
--(many others)
Clinically
Toxins that shouldn’t be ingested obvious
in large dz
quantities

Retina
for prolonged periods:
Which of these VF defects
--Ethanol
aresubtle
Clinically associated
dz with damage to each group?
--Tobacco Nasal step
Toxins you were told to ingest by a doc:
--Amiodarone
Papillomacular bundle Altitudinal
Temporal wedge
Optic nerve
--Ethambutol
--Isoniazid
Arcuate fibers Arcuate
Nasal radiating fibers
head --Linezolid
--(many others)
Central
Ceco-central
Nutrients that weren’t ingested in sufficient quantity:
--Vitamin B12
--Folate

Optic chiasm
--Thiamine
Inherited mitochondrial diseases:
--
Which
-- sorts of optic neuropathy are implicated if a P-M bundle VF defect is present?
Conditions involving compromised cellular metabolism: Think toxic/metabolic,
nutritional deficiencies, inherited mitochondrial dz, etc

Retrochiasmal
Why do conditions affecting metabolism preferentially affect the P-M bundle?
Because the P-M fibers are small, unmyelinated, and extremely active metabolically.
Taken together, these characteristics make them more vulnerable than the rest of
the optic nerve to factors that adversely impact metabolism.
74

Visual Field Defects


Toxins that shouldn’t be ingested at all:
--Methanol
--Ethylene glycol
--Lead (in children)
--(many others)
Clinically
Toxins that shouldn’t be ingested obvious
in large dz
quantities

Retina
for prolonged periods:
Which of these VF defects
--Ethanol
aresubtle
Clinically associated
dz with damage to each group?
--Tobacco Nasal step
Toxins you were told to ingest by a doc:
--Amiodarone
Papillomacular bundle Altitudinal
Temporal wedge
Optic nerve
--Ethambutol
--Isoniazid
Arcuate fibers Arcuate
Nasal radiating fibers
head --Linezolid
--(many others)
Central
Ceco-central
Nutrients that weren’t ingested in sufficient quantity:
--Vitamin B12
--Folate

Optic chiasm
--Thiamine
Inherited mitochondrial diseases:
--Leber’s hereditary optic neuropathy
Which sorts of optic
--Autosomal neuropathy
dominant are implicated if a P-M bundle VF defect is present?
optic atrophy
Conditions involving compromised cellular metabolism: Think toxic/metabolic,
nutritional deficiencies, inherited mitochondrial dz, etc

Retrochiasmal
Why do conditions affecting metabolism preferentially affect the P-M bundle?
Because the P-M fibers are small, unmyelinated, and extremely active metabolically.
Taken together, these characteristics make them more vulnerable than the rest of
the optic nerve to factors that adversely impact metabolism.
75

Visual Field Defects

Clinically obvious dz
Retina
Which of these VF defects aresubtle
Clinically associated
dz with damage to each group?
Nasal step
Papillomacular bundle Altitudinal
Temporal wedge
Optic nerve Arcuate fibers Arcuate
Nasal radiating fibers
head Central
Ceco-central

Optic chiasm
Which sorts of optic neuropathy are implicated if a P-M bundle VF defect is present?
Conditions involving compromised cellular metabolism: Think toxic/metabolic,
nutritional
In additiondeficiencies, inherited mitochondrial
to central/ceco-central dz, etc
VF defects, what other aspects of visual function
are invariably degraded by pathology affecting the P-M bundle?
Retrochiasmal
Why
-- do conditions affecting metabolism preferentially affect the P-M bundle?
Because
-- the P-M fibers are small, unmyelinated, and extremely active metabolically.
Taken together, these characteristics make them more vulnerable than the rest of
the optic nerve to factors that adversely impact metabolism.
76

Visual Field Defects

Clinically obvious dz
Retina
Which of these VF defects aresubtle
Clinically associated
dz with damage to each group?
Nasal step
Papillomacular bundle Altitudinal
Temporal wedge
Optic nerve Arcuate fibers Arcuate
Nasal radiating fibers
head Central
Ceco-central

Optic chiasm
Which sorts of optic neuropathy are implicated if a P-M bundle VF defect is present?
Conditions involving compromised cellular metabolism: Think toxic/metabolic,
nutritional
In additiondeficiencies, inherited mitochondrial
to central/ceco-central dz, etc
VF defects, what other aspects of visual function
are invariably degraded by pathology affecting the P-M bundle?
Retrochiasmal
Why do conditions
--Visual
Because
acuity*
--Color vision
affecting metabolism preferentially affect the P-M bundle?
the P-M fibers are*Which
small, makes
unmyelinated, and all,
sense—after extremely
a centralactive metabolically.
VF defect is present
Taken together, these characteristics make them more vulnerable than the rest of
the optic nerve to factors that adversely impact metabolism.
77

Visual Field Defects

Clinically obvious dz
Retina
Which of these VF defects aresubtle
Clinically associated
dz with damage to each group?
Nasal step
Papillomacular bundle Altitudinal
Temporal wedge
Optic nerve Arcuate fibers Arcuate
Nasal radiating fibers
head Central
Ceco-central

Optic chiasm
Which sorts of optic neuropathy are implicated if a P-M bundle VF defect is present?
Conditions involving compromised cellular metabolism: Think toxic/metabolic,
nutritional
In additiondeficiencies, inherited mitochondrial
to central/ceco-central dz, etc
VF defects, what other aspects of visual function
ForWhymore
are on
invariably PMB-related
degraded by pathologyoptic neuropathy,
affecting the P-M bundle? see slide-set N9
Retrochiasmal
do conditions
--Visual
Because
acuity*
--Color vision
affecting metabolism preferentially affect the P-M bundle?
the P-M fibers are*Which
small, makes
unmyelinated, and all,
sense—after extremely
a centralactive metabolically.
VF defect is present
Taken together, these characteristics make them more vulnerable than the rest of
the optic nerve to factors that adversely impact metabolism.
78

Visual Field Defects

Clinically obvious dz
Retina
Which of these VF defects aresubtle
Clinically associated
dz with damage to each group?
Nasal step
Papillomacular bundle Altitudinal
Temporal wedge ?
Optic nerve Arcuate fibers Arcuate

head Nasal radiating fibers Central


Ceco-central ?

Optic chiasm

Retrochiasmal
79

Visual Field Defects

Clinically obvious dz
Retina
Which of these VF defects aresubtle
Clinically associated
dz with damage to each group?
Nasal step
Papillomacular bundle Altitudinal
Temporal wedge
Optic nerve Arcuate fibers Arcuate
Nasal radiating fibers
head Central
Ceco-central

Optic chiasm

Retrochiasmal
80

Visual Field Defects

Clinically obvious dz
Retina
Which of these VF defects aresubtle
Clinically associated
dz with damage to each group?
Nasal step
Papillomacular bundle Altitudinal
Temporal wedge
Optic nerve Arcuate fibers Arcuate
Nasal radiating fibers
head Central
Ceco-central

Optic chiasm

If a pt presents with a VF defect c/w an arcuate fiber lesion,


what condition should you consider first?
Glaucoma
Retrochiasmal
Why does glaucoma preferentially damage arcuate fibers?
It’s unclear at this time
81

Visual Field Defects

Clinically obvious dz
Retina
Which of these VF defects aresubtle
Clinically associated
dz with damage to each group?
Nasal step
Papillomacular bundle Altitudinal
Temporal wedge
Optic nerve Arcuate fibers Arcuate
Nasal radiating fibers
head Central
Ceco-central

Optic chiasm

If a pt presents with a VF defect c/w an arcuate fiber lesion,


what condition should you consider first?
Glaucoma
Retrochiasmal
Why does glaucoma preferentially damage arcuate fibers?
It’s unclear at this time
82

Visual Field Defects

Clinically obvious dz
Retina
Which of these VF defects aresubtle
Clinically associated
dz with damage to each group?
Nasal step
Papillomacular bundle Altitudinal
Temporal wedge
Optic nerve Arcuate fibers Arcuate
Nasal radiating fibers
head Central
Ceco-central

Optic chiasm

If a pt presents with a VF defect c/w an arcuate fiber lesion,


what condition should you consider first?
Glaucoma
Retrochiasmal
Why does glaucoma preferentially damage arcuate fibers?
It’s unclear at this time
83

Visual Field Defects

Clinically obvious dz
Retina
Which of these VF defects aresubtle
Clinically associated
dz with damage to each group?
Nasal step
Papillomacular bundle Altitudinal
Temporal wedge
Optic nerve Arcuate fibers Arcuate
Nasal radiating fibers
head Central
Ceco-central

Optic chiasm

If a pt presents with a VF defect c/w an arcuate fiber lesion,


what condition should you consider first?
Glaucoma
Retrochiasmal
Why does glaucoma preferentially damage arcuate fibers?
It’s unclear at this time
84
Compare the distribution of arcuate-fiber defects with those associated with a P-M bundle dysfunction.
Visual Field Defects
What important difference do you see?
Unlike P-M defects, arcuate fiber bundle defects do not cross (ie, they ‘respect’) the horizontal midline

Why not?
Because fibers on the temporal side of the ONH approach, but do not cross, the horizontal midline. The
arcuate fibers arc around the P-M bundle, and meet along a horizontal demarcation line. Thus, damage
Clinically
to these fibers always result in VF defects obvious
that are limited dz the superior or the inferior portion of
to either
Retina
the field.
Which of these VF defects aresubtle
Clinically associated
dz with damage to each group?
What is this ‘horizontal demarcation line’ called? Nasal step
The horizontal raphe
Papillomacular bundle Altitudinal
Temporal wedge
Optic nerve Arcuate fibers Arcuate
Nasal radiating fibers
head Central
Ceco-central

Optic chiasm

Retrochiasmal
85
Compare the distribution of arcuate-fiber defects with those associated with a P-M bundle dysfunction.
Visual Field Defects
What important difference do you see?
Unlike P-M defects, arcuate fiber bundle defects do not cross (ie, they ‘respect’) the horizontal midline

Why not?
Because fibers on the temporal side of the ONH approach, but do not cross, the horizontal midline. The
arcuate fibers arc around the P-M bundle, and meet along a horizontal demarcation line. Thus, damage
Clinically
to these fibers always result in VF defects obvious
that are limited dz the superior or the inferior portion of
to either
Retina
the field.
Which of these VF defects aresubtle
Clinically associated
dz with damage to each group?
What is this ‘horizontal demarcation line’ called? Nasal step
The horizontal raphe
Papillomacular bundle Altitudinal
Temporal wedge
Optic nerve Arcuate fibers Arcuate
Nasal radiating fibers
head Central
Ceco-central

Optic chiasm

Retrochiasmal
86
Compare the distribution of arcuate-fiber defects with those associated with a P-M bundle dysfunction.
Visual Field Defects
What important difference do you see?
Unlike P-M defects, arcuate fiber bundle defects do not cross (ie, they ‘respect’) the horizontal midline

Why not?
Because fibers on the temporal side of the ONH approach, but do not cross, the horizontal midline. The
arcuate fibers arc around the P-M bundle, and meet along a horizontal demarcation line. Thus, damage
Clinically
to these fibers always result in VF defects obvious
that are limited dz the superior or the inferior portion of
to either
Retina
the field.
Which of these VF defects aresubtle
Clinically associated
dz with damage to each group?
What is this ‘horizontal demarcation line’ called? Nasal step
The horizontal raphe
Papillomacular bundle Altitudinal
Temporal wedge
Optic nerve Arcuate fibers Arcuate
Nasal radiating fibers
head Central
Ceco-central

Optic chiasm

Retrochiasmal
87
Compare the distribution of arcuate-fiber defects with those associated with a P-M bundle dysfunction.
Visual Field Defects
What important difference do you see?
Unlike P-M defects, arcuate fiber bundle defects do not cross (ie, they ‘respect’) the horizontal midline

Why not?
Because fibers on the temporal side of the ONH approach, but do not cross, the horizontal midline. The
arcuate fibers arc around the P-M bundle, and meet along a horizontal demarcation line. Thus,
Clinically
damage to these fibers always result in VF obvious
defects that dz to either the superior or the inferior
are limited
Retina
portion of the field.
Which of these VF defects aresubtle
Clinically associated
dz with damage to each group?
What is this ‘horizontal demarcation line’ called? Nasal step
The horizontal raphe
Papillomacular bundle Altitudinal
Temporal wedge
Optic nerve Arcuate fibers Arcuate
Nasal radiating fibers
head Central
Ceco-central

Optic chiasm

Retrochiasmal
88
Compare the distribution of arcuate-fiber defects with those associated with a P-M bundle dysfunction.
Visual Field Defects
What important difference do you see?
Unlike P-M defects, arcuate fiber bundle defects do not cross (ie, they ‘respect’) the horizontal midline

Why not?
Because fibers on the temporal side of the ONH approach, but do not cross, the horizontal midline. The
arcuate fibers arc around the P-M bundle, and meet along a horizontal demarcation line. Thus, damage
Clinically
to these fibers always result in VF defects obvious
that are limited dz the superior or the inferior portion of
to either
Retina
the field.
Which of these VF defects aresubtle
Clinically associated
dz with damage to each group?
What is this ‘horizontal demarcation line’ called? Nasal step
The horizontal raphe
Papillomacular bundle Altitudinal
Temporal wedge
Optic nerve Arcuate fibers Arcuate
Nasal radiating fibers
head Central
Ceco-central

Optic chiasm

Retrochiasmal
89
Compare the distribution of arcuate-fiber defects with those associated with a P-M bundle dysfunction.
Visual Field Defects
What important difference do you see?
Unlike P-M defects, arcuate fiber bundle defects do not cross (ie, they ‘respect’) the horizontal midline

Why not?
Because fibers on the temporal side of the ONH approach, but do not cross, the horizontal midline. The
arcuate fibers arc around the P-M bundle, and meet along a horizontal demarcation line. Thus, damage
Clinically
to these fibers always result in VF defects obvious
that are limited dz the superior or the inferior portion of
to either
Retina
the field.
Which of these VF defects aresubtle
Clinically associated
dz with damage to each group?
What is this horizontal demarcation line called? Nasal step
The horizontal raphe
Papillomacular bundle Altitudinal
Temporal wedge
Optic nerve Arcuate fibers Arcuate
Nasal radiating fibers
head Central
Ceco-central

Optic chiasm
?

Retrochiasmal
90
Compare the distribution of arcuate-fiber defects with those associated with a P-M bundle dysfunction.
Visual Field Defects
What important difference do you see?
Unlike P-M defects, arcuate fiber bundle defects do not cross (ie, they ‘respect’) the horizontal midline

Why not?
Because fibers on the temporal side of the ONH approach, but do not cross, the horizontal midline. The
arcuate fibers arc around the P-M bundle, and meet along a horizontal demarcation line. Thus, damage
Clinically
to these fibers always result in VF defects obvious
that are limited dz the superior or the inferior portion of
to either
Retina
the field.
Which of these VF defects aresubtle
Clinically associated
dz with damage to each group?
What is this horizontal demarcation line called? Nasal step
The horizontal raphe
Papillomacular bundle Altitudinal
Temporal wedge
Optic nerve Arcuate fibers Arcuate
Nasal radiating fibers
head Central
Ceco-central

Optic chiasm
‘Horizontal raphe’

Retrochiasmal
91

Visual Field Defects

Clinically obvious dz
Retina
Which of these VF defects aresubtle
Clinically associated
dz with damage to each group?
Nasal step
Papillomacular bundle Altitudinal
Temporal wedge ?
Optic nerve Arcuate fibers Arcuate

head Nasal radiating fibers Central


Ceco-central ?

Optic chiasm

Retrochiasmal
92

Visual Field Defects

Clinically obvious dz
Retina
Which of these VF defects aresubtle
Clinically associated
dz with damage to each group?
Nasal step
Papillomacular bundle Altitudinal
Temporal wedge
Optic nerve Arcuate fibers Arcuate
Nasal radiating fibers
head Central
Ceco-central

Optic chiasm

Retrochiasmal
93

Visual Field Defects

Clinically obvious dz
Retina
Which of these VF defects aresubtle
Clinically associated
dz with damage to each group?
Nasal step
Papillomacular bundle Altitudinal
Temporal wedge ?
Optic nerve Arcuate fibers Arcuate
Nasal radiating fibers
head Central
Ceco-central

Optic chiasm
If a pt presents with an altitudinal VF defect, what condition should you consider first?
Two conditions should come to mind:
--If the pt is a 50+ vasculopath , it’s likely nonarteritic anterior ischemic optic neuropathy (NAION)
--If the pt has glaucoma, it likely represents advanced glaucomatous optic neuropathy
Retrochiasmal
How can you differentiate between these two conditions?
There are a number of ways, but the most straightforward would be to inspect the ONH, which will
be edematous in NAION, and severely cupped in advanced glaucoma
94

Visual Field Defects

Clinically obvious dz
Retina
Which of these VF defects aresubtle
Clinically associated
dz with damage to each group?
Nasal step
Papillomacular bundle Altitudinal
Temporal wedge ?
Optic nerve Arcuate fibers Arcuate
Nasal radiating fibers
head Central
Ceco-central

Optic chiasm
If a pt presents with an altitudinal VF defect, what condition should you consider first?
Two conditions should come to mind:
--
--If the pt has glaucoma, it likely represents advanced glaucomatous optic neuropathy
Retrochiasmal
How can you differentiate between these two conditions?
There are a number of ways, but the most straightforward would be to inspect the ONH, which will
be edematous in NAION, and severely cupped in advanced glaucoma
95

Visual Field Defects

Clinically obvious dz
Retina
Which of these VF defects aresubtle
Clinically associated
dz with damage to each group?
Nasal step
Papillomacular bundle Altitudinal
Temporal wedge ?
Optic nerve Arcuate fibers Arcuate
Nasal radiating fibers
head Central
Ceco-central

Optic chiasm
If a pt presents with an altitudinal VF defect, what condition should you consider first?
Two conditions should come to mind:
--If the pt is a 50+
agevasculopath
and condition , it’s likely nonarteritic anterior ischemic optic neuropathy (NAION)
--If the pt has glaucoma, it likely represents advanced glaucomatous optic neuropathy
Retrochiasmal
How can you differentiate between these two conditions?
There are a number of ways, but the most straightforward would be to inspect the ONH, which will
be edematous in NAION, and severely cupped in advanced glaucoma
96

Visual Field Defects

Clinically obvious dz
Retina
Which of these VF defects aresubtle
Clinically associated
dz with damage to each group?
Nasal step
Papillomacular bundle Altitudinal
Temporal wedge ?
Optic nerve Arcuate fibers Arcuate
Nasal radiating fibers
head Central
Ceco-central

Optic chiasm
If a pt presents with an altitudinal VF defect, what condition should you consider first?
Two conditions should come to mind:
--If the pt is a 50+ vasculopath , it’s likely nonarteritic anterior ischemic optic neuropathy (NAION)
--If the pt has glaucoma, it likely represents advanced glaucomatous optic neuropathy
Retrochiasmal
How can you differentiate between these two conditions?
There are a number of ways, but the most straightforward would be to inspect the ONH, which will
be edematous in NAION, and severely cupped in advanced glaucoma
97

Visual Field Defects

Clinically obvious dz
Retina
Which of these VF defects aresubtle
Clinically associated
dz with damage to each group?
Nasal step
Papillomacular bundle Altitudinal
Temporal wedge ?
Optic nerve Arcuate fibers Arcuate
Nasal radiating fibers
head Central
Ceco-central

Optic chiasm
If a pt presents with an altitudinal VF defect, what condition should you consider first?
Two conditions should come to mind:
--If the pt is a 50+ vasculopath , it’s likely nonarteritic anterior ischemic optic neuropathy (NAION)
--If the pt has glaucoma, it likely represents advanced glaucomatous optic neuropathy
Retrochiasmal
How can you differentiate between these two conditions?
There are a number of ways, but the most straightforward would be to inspect the ONH, which will
be edematous in NAION, and severely cupped in advanced glaucoma
98

Visual Field Defects

Clinically obvious dz
Retina
Which of these VF defects aresubtle
Clinically associated
dz with damage to each group?
Nasal step
Papillomacular bundle Altitudinal
Temporal wedge ?
Optic nerve Arcuate fibers Arcuate
Nasal radiating fibers
head Central
Ceco-central

Optic chiasm
If a pt presents with an altitudinal VF defect, what condition should you consider first?
Two conditions should come to mind:
--If the pt is a 50+ vasculopath , it’s likely nonarteritic anterior ischemic optic neuropathy (NAION)
--If the pt has glaucoma, it likely represents advanced glaucomatous optic neuropathy
Retrochiasmal
How can you differentiate between these two conditions?
There are a number of ways, but the most straightforward would be to inspect the ONH, which will
be edematous
one word in NAION, and severely cupped in advanced glaucoma
two words
99

Visual Field Defects

Clinically obvious dz
Retina
Which of these VF defects aresubtle
Clinically associated
dz with damage to each group?
Nasal step
Papillomacular bundle Altitudinal
Temporal wedge ?
Optic nerve Arcuate fibers Arcuate
Nasal radiating fibers
head Central
Ceco-central

Optic chiasm
If a pt presents with an altitudinal VF defect, what condition should you consider first?
Two conditions should come to mind:
--If the pt is a 50+ vasculopath , it’s likely nonarteritic anterior ischemic optic neuropathy (NAION)
--If the pt has glaucoma, it likely represents advanced glaucomatous optic neuropathy
Retrochiasmal
How can you differentiate between these two conditions?
There are a number of ways, but the most straightforward would be to inspect the ONH, which will
be edematous in NAION, and severely cupped in advanced glaucoma
100

Visual Field Defects

Clinically obvious dz
Retina Clinically subtle dz
Nasal step
Depressions Altitudinal
Temporal wedge
Optic nerve Arcuate
Scotomas Central
Ceco-central

Bitemporal hemianopia
Binasal
fourhemianopia
very specific
Optic chiasm types of chiasmal
Junctional common
VF defects
Junctional rare

Retrochiasmal
101

Visual Field Defects

Clinically obvious dz
Retina Clinically subtle dz
Nasal step
Depressions Altitudinal
Temporal wedge
Optic nerve Arcuate
Scotomas Central
Ceco-central

Bitemporal hemianopia
Binasal hemianopia
Optic chiasm Junctional common
Junctional rare

Retrochiasmal
102

Visual Field Defects

Clinically obvious dz
Retina Clinically subtle dz
Nasal step
Depressions Altitudinal
Temporal wedge
Optic nerve Arcuate
Scotomas Central
Ceco-central

Bitemporal hemianopia
Binasal hemianopia
Optic chiasm Junctional common
Junctional rare

Optic tract
four fairly specific
LGN
Retrochiasmal retrochiasmal anatomic
Opticlocations associated
radiations
with VF defects
Occipital cortex
103

Visual Field Defects

Clinically obvious dz
Retina Clinically subtle dz
Nasal step
Depressions Altitudinal
Temporal wedge
Optic nerve Arcuate
Scotomas Central
Ceco-central

Bitemporal hemianopia
Binasal hemianopia
Optic chiasm Junctional common
Junctional rare

Optic tract
LGN
Retrochiasmal Optic radiations
Occipital cortex
104

Visual Field Defects

Clinically obvious dz
Retina Clinically subtle dz
Nasal step
Depressions Altitudinal
Temporal wedge
Optic nerve Arcuate
Forget
Forget Scotomas
all
all of
of these
these specific
specificCentral
VF
VF findings
findings
for
for just
just aa minute…In
minute…In the Ceco-central
the most
most general
general
of
of terms,
terms, what
what can
can we
we say
say about
about VFVF
defects
defects associated
associated with
with lesions
lesions in
in
eachBitemporal
each of
of these hemianopia
these locations?
locations?
Binasal hemianopia
Optic chiasm Junctional common
Junctional rare

Optic tract
LGN
Retrochiasmal Optic radiations
Occipital cortex
105

Visual Field Defects


VF defect

(Start here)
Clinically obvious dz
Retina Clinically subtle dz ?
Nasal step
Depressions Altitudinal
Temporal wedge
Optic nerve
ForgetScotomas
Arcuate
all of these specificCentral
VF findings
Ceco-central
?
for just a minute…In the most general
of terms, what can we say about VF
defects associated with lesions in
each Bitemporal hemianopia
of these locations?

Optic chiasm
Binasal hemianopia
Junctional common
?
Junctional rare

Optic tract
Retrochiasmal LGN
Optic radiations
?
Occipital cortex
106

Visual Field Defects


VF defect

Clinically obvious dz Anything except


a vertical
Retina Clinically subtle dz
meridian cut
(unless by pure
chance)
Nasal step
Depressions Altitudinal
Temporal wedge Anything except
Optic nerve
?
a vertical
Arcuate meridian cut
ForgetScotomas
all of these specificCentral
VF findings (unless by pure
Ceco-central chance)
for just a minute…In the most general
of terms, what can we say about VF
defects associated with lesions in
eachBitemporal hemianopia
of these locations? With few

Optic chiasm
Binasal hemianopia
Junctional common
?
exceptions, will
not cross the
vertical meridian
Junctional rare

Optic tract With few

Retrochiasmal LGN
Optic radiations
?
exceptions, must
be homonymous
hemianopia-like

Occipital cortex
107

Visual Field Defects


VF defect

Clinically obvious dz Anything except


a vertical
Retina Clinically subtle dz
meridian cut
(unless by pure
chance)
Nasal step
Depressions Altitudinal (Next)
Temporal wedge Anything except
Optic nerve
?
a vertical
Arcuate meridian cut
ForgetScotomas
all of these specificCentral
VF findings (unless by pure
Ceco-central chance)
for just a minute…In the most general
of terms, what can we say about VF
defects associated with lesions in
eachBitemporal hemianopia
of these locations? With few

Optic chiasm
Binasal hemianopia
Junctional common
?
exceptions, will
not cross the
vertical meridian
Junctional rare

Optic tract With few

Retrochiasmal LGN
Optic radiations
?
exceptions, must
be homonymous
hemianopia-like

Occipital cortex
108

Visual Field Defects


VF defect

Clinically obvious dz Anything except


a vertical
Retina Clinically subtle dz
meridian cut
(unless by pure
chance)
Nasal step
Depressions Altitudinal
Temporal wedge Anything except
Optic nerve Arcuate
a vertical
meridian cut
ForgetScotomas
all of these specificCentral
VF findings (unless by pure
Ceco-central chance)
for just a minute…In the most general
of terms, what can we say about VF
defects associated with lesions in
eachBitemporal hemianopia
of these locations? With few

Optic chiasm
Binasal hemianopia
Junctional common
?
exceptions, will
not cross the
vertical meridian
Junctional rare

Optic tract With few

Retrochiasmal LGN
Optic radiations
?
exceptions, must
be homonymous
hemianopia-like

Occipital cortex
109

Visual Field Defects


VF defect

Clinically obvious dz Anything except


a vertical
Retina Clinically subtle dz
meridian cut
(unless by pure
chance)
Nasal step
Depressions Altitudinal
Temporal wedge Anything except
Optic nerve Arcuate
a vertical
meridian cut
ForgetScotomas
all of these specificCentral
VF findings (unless by pure
Ceco-central chance)
for just a minute…In the most general
of terms, what can we say about VF
defects associated with lesions in (Next)
eachBitemporal hemianopia
of these locations? With few

Optic chiasm
Binasal hemianopia
Junctional common
?
exceptions, will
not cross the
vertical meridian
Junctional rare

Optic tract With few

Retrochiasmal LGN
Optic radiations
?
exceptions, must
be homonymous
hemianopia-like

Occipital cortex
110

Visual Field Defects


VF defect

Clinically obvious dz Anything except


a vertical
Retina Clinically subtle dz
meridian cut
(unless by pure
chance)
Nasal step
Depressions Altitudinal
Temporal wedge Anything except
Optic nerve Arcuate
a vertical
meridian cut
ForgetScotomas
all of these specificCentral
VF findings (unless by pure
Ceco-central chance)
for just a minute…In the most general
of terms, what can we say about VF
defects associated with lesions in
eachBitemporal hemianopia
of these locations? With few
Binasal hemianopia exceptions, will
Optic chiasm Junctional common
not cross the
vertical meridian
Junctional rare

Optic tract With few

Retrochiasmal LGN
Optic radiations
?
exceptions, must
be homonymous
hemianopia-like

Occipital cortex
111

Visual Field Defects


VF defect

Clinically obvious dz Anything except


a vertical
Retina Clinically subtle dz
meridian cut
(unless by pure
chance)
Nasal step
Depressions Altitudinal
Temporal wedge Anything except
Optic nerve Arcuate
a vertical
meridian cut
ForgetScotomas
all of these specificCentral
VF findings (unless by pure
Ceco-central chance)
for just a minute…In the most general
of terms, what can we say about VF
defects associated with lesions in
eachBitemporal hemianopia
of these locations? With few
Binasal hemianopia exceptions, will
Optic chiasm Junctional common
not cross the
vertical meridian
Junctional rare
(Next)
Optic tract With few

Retrochiasmal LGN
Optic radiations
?
exceptions, must
be homonymous
hemianopia-like

Occipital cortex
112

Visual Field Defects


VF defect

Clinically obvious dz Anything except


a vertical
Retina Clinically subtle dz
meridian cut
(unless by pure
chance)
Nasal step
Depressions Altitudinal
Temporal wedge Anything except
Optic nerve Arcuate
a vertical
meridian cut
ForgetScotomas
all of these specificCentral
VF findings (unless by pure
Ceco-central chance)
for just a minute…In the most general
of terms, what can we say about VF
defects associated with lesions in
eachBitemporal hemianopia
of these locations? With few
Binasal hemianopia exceptions, will
Optic chiasm Junctional common
not cross the
vertical meridian
Junctional rare

Optic tract With few


exceptions,
LGN must be
Retrochiasmal Optic radiations
homonymous
hemianopia-like

Occipital cortex
113

Visual Field Defects

Clinically obvious dz
Retina Clinically subtle dz
Nasal step
Depressions Altitudinal
Temporal wedge
Optic nerve Arcuate
Scotomas Central
Ceco-central

Bitemporal hemianopia
Binasal hemianopia
Optic chiasm Junctional common
In basic terms, what is the difference between chiasmal
Junctional rare in a bitemporal VF defect vs those
lesions resulting
producing a binasal defect?
Optic tract defects are the result of a lesion impacting
Bitemporal
LGNthe central portion of the chiasm, whereas binasal
Retrochiasmal defects stem from lesions affecting the lateral portions
Optic radiations
of the chiasm
Occipital cortex
114

Visual Field Defects

Clinically obvious dz
Retina Clinically subtle dz
Nasal step
Depressions Altitudinal
Temporal wedge
Optic nerve Arcuate
Scotomas Central
Ceco-central

Bitemporal hemianopia: Central aspect of chiasm


Binasal hemianopia: Lateral portions of chiasm
Optic chiasm Junctional common
In basic terms, what is the difference between chiasmal
Junctional rare in a bitemporal VF defect vs those
lesions resulting
producing a binasal defect?
Optic tract defects are the result of a lesion impacting
Bitemporal
LGNthe central portion of the chiasm, whereas binasal
Retrochiasmal defects stem from lesions affecting the lateral portions
Optic radiations
of the chiasm
Occipital cortex
115

Here’s why:

Bitemporal hemianopia: Central aspect of chiasm


Binasal hemianopia: Lateral portions of chiasm
In basic terms, what is the difference between chiasmal
lesions resulting in a bitemporal VF defect vs those
producing a binasal defect?

Bitemporal defects are the result of a lesion impacting


the central portion of the chiasm, whereas binasal
defects stem from lesions affecting the lateral portions
of the chiasm
116

Temporal VF Temporal VF
The nasal retinas are responsible
for the temporal visual fields.

Here’s why:

Bitemporal hemianopia: Central aspect of chiasm


Binasal hemianopia: Lateral portions of chiasm
In basic terms, what is the difference between chiasmal
lesions resulting in a bitemporal VF defect vs those
producing a binasal defect?

Bitemporal defects are the result of a lesion impacting


the central portion of the chiasm, whereas binasal
defects stem from lesions affecting the lateral portions
of the chiasm
117

Temporal VF Temporal VF
The nasal retinas are responsible
for the temporal visual fields.

Here’s why:

Optic
Bitemporal hemianopia: Central aspect of chiasm
Binasal hemianopia: Lateral portions of chiasm
Chiasm
In basic terms, what is the difference between chiasmal
lesions resulting in a bitemporal VF defect vs those
producing a binasal defect?
Fibers originating Bitemporal defects are the result of a lesion impacting
in the nasal retinas the central portion of the chiasm, whereas binasal
cross at the chiasm. defects stem from lesions affecting the lateral portions
of the chiasm
118

Temporal VF Temporal VF
The nasal retinas are responsible
for the temporal visual fields.

Here’s why:
So a lesion of the central chiasm will bag
these fibers, and thus tend to cause
bitemporal defects

Optic
Bitemporal hemianopia: Central aspect of chiasm
Binasal hemianopia: Lateral portions of chiasm
Chiasm
In basic terms, what is the difference between chiasmal
lesions resulting in a bitemporal VF defect vs those
producing a binasal defect?
Fibers originating Bitemporal defects are the result of a lesion impacting
in the nasal retinas the central portion of the chiasm, whereas binasal
cross at the chiasm. defects stem from lesions affecting the lateral portions
of the chiasm
119

The temporal retinas are responsible


for the nasal visual fields.

Nasal VF Nasal VF

Here’s why:

Bitemporal hemianopia: Central aspect of chiasm


Binasal hemianopia: Lateral portions of chiasm
In basic terms, what is the difference between chiasmal
lesions resulting in a bitemporal VF defect vs those
producing a binasal defect?

Bitemporal defects are the result of a lesion impacting


the central portion of the chiasm, whereas binasal
defects stem from lesions affecting the lateral portions
of the chiasm
120

The temporal retinas are responsible


for the nasal visual fields.

Nasal VF Nasal VF

Here’s why:

Optic
Bitemporal hemianopia: Central aspect of chiasm
Binasal hemianopia: Lateral portions of chiasm
Chiasm
In basic terms, what is the difference between chiasmal
lesions resulting in a bitemporal VF defect vs those
producing a binasal defect?
Fibers originating Bitemporal defects are the result of a lesion impacting
in the temporal the central portion of the chiasm, whereas binasal
retinas do not cross defects stem from lesions affecting the lateral portions
of the chiasm
at the chiasm.
121

The temporal retinas are responsible


for the nasal visual fields.

Nasal VF Nasal VF

Here’s why:
So lesions of the central chiasm will miss
these fibers… lesions of the lateral
chiasm will bag them, thereby causing
binasal defects (note that two lesions are
required
Bitemporal to do this)Central aspect of chiasm
hemianopia:
Optic
Binasal hemianopia: Lateral portions of chiasm
Chiasm
In basic terms, what is the difference between chiasmal
lesions resulting in a bitemporal VF defect vs those
producing a binasal defect?
Fibers originating Bitemporal defects are the result of a lesion impacting
in the temporal the central portion of the chiasm, whereas binasal
retinas do not cross defects stem from lesions affecting the lateral portions
of the chiasm
at the chiasm.
122

The temporal retinas are responsible


for the nasal visual fields.

Nasal VF Nasal VF

Here’s why:
So lesions of the central chiasm will miss
these fibers…But lesions of the lateral
chiasm will bag them, thereby causing
binasal defects (note that two lesions are
required
Bitemporal to do this)Central aspect of chiasm
hemianopia:
Optic
Binasal hemianopia: Lateral portions of chiasm
Chiasm
In basic terms, what is the difference between chiasmal
lesions resulting in a bitemporal VF defect vs those
producing a binasal defect?
Fibers originating Bitemporal defects are the result of a lesion impacting
in the temporal the central portion of the chiasm, whereas binasal
retinas do not cross defects stem from lesions affecting the lateral portions
of the chiasm
at the chiasm.
123

The temporal retinas are responsible


for the nasal visual fields.
What structures are located at the lateral
Nasal VF Nasal VF
aspects of the chiasm?
The internal carotid arteries

Here’s why:
So lesions of the central chiasm will miss
these fibers…But lesions of the lateral
chiasm will bag them, thereby causing
binasal defects (note that two lesions are
required
Bitemporal to do this)Central aspect of chiasm
hemianopia:
Optic

? ? Binasal hemianopia: Lateral portions of chiasm


Chiasm
In basic terms, what is the difference between chiasmal
lesions resulting in a bitemporal VF defect vs those
producing a binasal defect?
Fibers originating Bitemporal defects are the result of a lesion impacting
in the temporal the central portion of the chiasm, whereas binasal
retinas do not cross defects stem from lesions affecting the lateral portions
of the chiasm
at the chiasm.
124

The temporal retinas are responsible


for the nasal visual fields.
What structures are located at the lateral
Nasal VF Nasal VF
aspects of the chiasm?
The internal carotid arteries

Here’s why:
So lesions of the central chiasm will miss
these fibers…But lesions of the lateral
chiasm will bag them, thereby causing
binasal defects (note that two lesions are
required
Bitemporal to do this)Central aspect of chiasm
hemianopia:
Optic
Binasal hemianopia: Lateral portions of chiasm
Chiasm
In basic terms, what is the difference between chiasmal
lesions resulting in a bitemporal VF defect vs those
producing a binasal defect?
Fibers originating Bitemporal defects are the result of a lesion impacting
in the temporal the central portion of the chiasm, whereas binasal
retinas do not cross defects stem from lesions affecting the lateral portions
of the chiasm
at the chiasm.
125

Visual Field Defects

What is the classic cause of a bitemporal hemianopia?


Pituitary adenoma
Clinically obvious dz
Retina Is the hemianopia usually inferior, superior or complete?
Clinically subtle dz
Superior
Nasal step
Why usually superior?
Depressions
The pituitary gland
Altitudinal
is belowwedge
the chiasm, therefore, pituitary
Temporal
Optic nerve lesions affect the inferior chiasmal fibers primarily. These
fibers account forArcuate
the superior VF.
Scotomas Central
Ceco-central
Is it usually congruous or incongruous?
Incongruous

Bitemporal hemianopia
Binasal hemianopia
Optic chiasm Junctional common
Junctional rare

Optic tract
LGN
Retrochiasmal Optic radiations
Occipital cortex
126

Visual Field Defects

What is the classic cause of a bitemporal hemianopia?


Pituitary adenoma
Clinically obvious dz
Retina Is the hemianopia usually inferior, superior or complete?
Clinically subtle dz
Superior
Nasal step
Why usually superior?
Depressions
The pituitary gland
Altitudinal
is belowwedge
the chiasm, therefore, pituitary
Temporal
Optic nerve lesions affect the inferior chiasmal fibers primarily. These
fibers account forArcuate
the superior VF.
Scotomas Central
Ceco-central
Is it usually congruous or incongruous?
Incongruous

Bitemporal hemianopia
Binasal hemianopia
Optic chiasm Junctional common
Junctional rare

Optic tract
LGN
Retrochiasmal Optic radiations
Occipital cortex
127

Visual Field Defects

What is the classic cause of a bitemporal hemianopia?


Pituitary adenoma
Clinically obvious dz
Retina Is the hemianopia usually inferior, superior or complete?
Clinically subtle dz
Superior
Nasal step
Why usually superior?
Depressions
The pituitary gland
Altitudinal
is belowwedge
the chiasm, therefore, pituitary
Temporal
Optic nerve lesions affect the inferior chiasmal fibers primarily. These
fibers account forArcuate
the superior VF.
Scotomas Central
Ceco-central
Is it usually congruous or incongruous?
Incongruous

Bitemporal hemianopia
Binasal hemianopia
Optic chiasm Junctional common
Junctional rare

Optic tract
LGN
Retrochiasmal Optic radiations
Occipital cortex
128

Visual Field Defects

What is the classic cause of a bitemporal hemianopia?


Pituitary adenoma
Clinically obvious dz
Retina Is the hemianopia usually inferior, superior or complete?
Clinically subtle dz
Superior
Nasal step
Why usually superior?
Depressions
The pituitary gland
Altitudinal
is belowwedge
the chiasm, therefore, pituitary
Temporal
Optic nerve lesions affect the inferior chiasmal fibers primarily. These
fibers account forArcuate
the superior VF.
Scotomas Central
Ceco-central
Is it usually congruous or incongruous?
Incongruous

Bitemporal hemianopia
Binasal hemianopia
Optic chiasm Junctional common
Junctional rare

Optic tract
LGN
Retrochiasmal Optic radiations
Occipital cortex
129

Visual Field Defects

What is the classic cause of a bitemporal hemianopia?


Pituitary adenoma
Clinically obvious dz
Retina Is the hemianopia usually inferior, superior or complete?
Clinically subtle dz
Superior
Nasal step
Why usually superior?
Depressions
The pituitary gland
Altitudinal
is belowwedge
the chiasm, therefore, pituitary
Temporal
Optic nerve lesions affect the inferior chiasmal fibers primarily. These
fibers account forArcuate
the superior VF.
Scotomas Central
Ceco-central
Is it usually congruous or incongruous?
Incongruous

Bitemporal hemianopia
Binasal hemianopia
Optic chiasm Junctional common
Junctional rare

Optic tract
LGN
Retrochiasmal Optic radiations
Occipital cortex
130

Visual Field Defects

What is the classic cause of a bitemporal hemianopia?


OD OS Pituitary adenoma
Clinically obvious dz
Retina Is the hemianopia usually inferior, superior or complete?
Clinically subtle dz
Superior
Nasal step
Why usually superior?
Depressions
The pituitary gland
Altitudinal
is belowwedge
the chiasm, therefore, pituitary
Temporal
Optic nerve
Pituitary
Optic lesions affect the inferior chiasmal fibers primarily. These
fibers account forArcuate
the superior visual field.
gland
Scotomas Central
Chiasm Ceco-central
Is it usually congruous or incongruous?
(viewed from below)
Incongruous

Bitemporal hemianopia
Binasal hemianopia
Optic chiasm Junctional common
Junctional rare

Optic tract
LGN
Retrochiasmal Optic radiations
Occipital cortex
131

Visual Field Defects

What is the classic cause of a bitemporal hemianopia?


Pituitary adenoma
Clinically obvious dz
Retina Is the hemianopia usually inferior, superior or complete?
Clinically subtle dz
Superior
Nasal step
Why usually superior?
Depressions
The pituitary gland
Altitudinal
is belowwedge
the chiasm, therefore, pituitary
Temporal
Optic nerve lesions affect the inferior chiasmal fibers primarily. These
fibers account forArcuate
the superior visual field.
Scotomas Central
Ceco-central
Is it usually congruous or incongruous?
Incongruous

Bitemporal hemianopia
Binasal hemianopia
Optic chiasm Junctional common
Junctional rare

Optic tract
LGN
Retrochiasmal Optic radiations
Occipital cortex
132

Visual Field Defects

What is the classic cause of a bitemporal hemianopia?


Pituitary adenoma
Clinically obvious dz
Retina Is the hemianopia usually inferior, superior or complete?
Clinically subtle dz
Superior
Nasal step
Why usually superior?
Depressions
The pituitary gland
Altitudinal
is belowwedge
the chiasm, therefore, pituitary
Temporal
Optic nerve lesions affect the inferior chiasmal fibers primarily. These
fibers account forArcuate
the superior visual field.
Scotomas Central
Ceco-central
Is it usually congruous or incongruous?
Incongruous

Bitemporal hemianopia
Binasal hemianopia
Optic chiasm Junctional common
Junctional rare

Optic tract
LGN
Retrochiasmal Optic radiations
Occipital cortex
133

Visual Field Defects

Clinically obvious dz
Retina Clinically subtle dz
Nasal step
Depressions Altitudinal
Temporal wedge
Optic nerve Arcuate
Scotomas Central
Ceco-central

Bitemporal hemianopia
Binasal hemianopia
Optic chiasm Junctional common
What is the classic cause of a chiasmal
Junctional rarebinasal hemianopia?
Bilateral carotid disease

What is the actual etiology


Opticfor tract
the vast majority of real-world binasal defects?
Glaucoma
LGN
Retrochiasmal Optic radiations
Occipital cortex
134

Visual Field Defects


OD OS

Clinically obvious dz
Retina
Optic
Clinically subtle dz
Nasal step
Depressions Altitudinal
Chiasm Temporal wedge
Optic nerve Arcuate
Scotomas Central
Ceco-central

Bitemporal hemianopia
Binasal hemianopia
Optic chiasm Junctional common
What is the classic cause of a chiasmal
Junctional rarebinasal hemianopia?
Bilateral carotid atherosclerotic dz compressing the outer chiasm bilaterally

What is the actual etiology


Opticfor tract
the vast majority of real-world binasal defects?
Glaucoma
LGN
Retrochiasmal Optic radiations
Occipital cortex
135

Visual Field Defects

Clinically obvious dz
Retina Clinically subtle dz
Nasal step
Depressions Altitudinal
Temporal wedge
Optic nerve Arcuate
Scotomas Central
Ceco-central

Bitemporal hemianopia
Binasal hemianopia
Optic chiasm Junctional common
What is the classic cause of a chiasmal
Junctional rarebinasal hemianopia?
Bilateral carotid atherosclerotic dz compressing the outer chiasm bilaterally

What is the actual etiology


Opticfor tract
the vast majority of real-world binasal defects?
Glaucoma
LGN
Retrochiasmal Optic radiations
Occipital cortex
136

Visual Field Defects

Clinically obvious dz
Retina Clinically subtle dz
Nasal step
Depressions Altitudinal
Temporal wedge
Optic nerve Arcuate
Scotomas Central
Ceco-central

Bitemporal hemianopia
Binasal hemianopia
Optic chiasm Junctional common
What is the classic cause of a chiasmal
Junctional rarebinasal hemianopia?
Bilateral carotid atherosclerotic dz compressing the outer chiasm bilaterally

What is the actual etiology


Opticfor tract
the vast majority of real-world binasal defects?
Glaucoma
LGN
Retrochiasmal Optic radiations
Occipital cortex
137

Visual Field Defects

Clinically obvious dz
Retina Clinically subtle dz
Nasal step
Depressions Altitudinal
Temporal wedge
Optic nerve Arcuate
Scotomas Central
Ceco-central

Bitemporal hemianopia
Binasal hemianopia
Optic chiasm Junctional common
Junctional rare
What does the term junctional refer to anatomically?
The junction between the optic nerve and the chiasm
Optic tract
What does a junctional common VF defect look like?
LGN
Retrochiasmal
An optic nerve VF defect in one eye and a hemianopic-like defect in the other
Optic radiations
Occipital cortex
138

Visual Field Defects

Clinically obvious dz
Retina Clinically subtle dz
Nasal step
Depressions Altitudinal
Temporal wedge
Optic nerve Arcuate
Scotomas Central
Ceco-central

Bitemporal hemianopia
Binasal hemianopia
Optic chiasm Junctional common
Junctional rare
What does the term junctional refer to anatomically?
The junction between the optic nerve and the chiasm
Optic tract
What does a junctional common VF defect look like?
LGN
Retrochiasmal
An optic nerve VF defect in one eye and a hemianopic-like defect in the other
Optic radiations
Occipital cortex
139

Visual Field Defects

Clinically obvious dz
Retina Clinically subtle dz
Nasal step
Depressions Altitudinal
Temporal wedge
Optic nerve Arcuate
Scotomas Central
Ceco-central

Bitemporal hemianopia
Binasal hemianopia
Optic chiasm Junctional common
Junctional rare
What does the term junctional refer to anatomically?
The junction between the optic nerve and the chiasm
Optic tract
What does a junctional common VF defect look like?
LGN
Retrochiasmal
An optic nerve VF defect in one eye and a hemianopic-like defect in the other
Optic radiations
Occipital cortex
140

Visual Field Defects

Clinically obvious dz
Retina Clinically subtle dz
Nasal step
Depressions Altitudinal
Temporal wedge
Optic nerve Arcuate
Scotomas Central
Ceco-central

Bitemporal hemianopia
Binasal hemianopia
Optic chiasm Junctional common
Junctional rare
What does the term junctional refer to anatomically?
The junction between the optic nerve and the chiasm
Optic tract
What does a junctional common VF defect look like?
LGN
Retrochiasmal
An optic nerve VF defect in one eye and a hemianopic-like defect in the other
Optic radiations
Occipital cortex i.e., it respects the vertical meridian
141

Visual Field Defects

Clinically obvious dz
Retina Clinically subtle dz
Nasal step
Depressions Altitudinal
Temporal wedge
Optic nerve Arcuate
Scotomas Central
Ceco-central

Bitemporal hemianopia
Binasal hemianopia
Optic chiasm Junctional common
Junctional rare

Optic tract
What does a junctional rare VF defect look like?
A hemianopic-like defectLGN
Retrochiasmal in one eye, but no lesion in the other
Optic radiations
Occipital cortex
142

Visual Field Defects

Clinically obvious dz
Retina Clinically subtle dz
Nasal step
Depressions Altitudinal
Temporal wedge
Optic nerve Arcuate
Scotomas Central
Ceco-central

Bitemporal hemianopia
Binasal hemianopia
Optic chiasm Junctional common
Junctional rare

Optic tract
What does a junctional rare VF defect look like?
A hemianopic-like defectLGN
Retrochiasmal in one eye, but no lesion in the other
Optic radiations
Occipital cortex
143

Visual Field Defects


VF defect

Clinically obvious dz Anything except


a vertical
Retina Clinically subtle dz
meridian cut
(unless by pure
chance)
Nasal step
Depressions Altitudinal
Temporal wedge Anything except
Optic nerve Arcuate
a vertical
meridian cut
ForgetScotomas
all of these specificCentral
VF findings (unless by pure
Ceco-central chance)
for just a minute…In the most general
of terms, what can we say about VF
defects associated with lesions in
eachBitemporal hemianopia
of these locations? With few
Binasal hemianopia exceptions, will
Optic chiasm Junctional common
not cross the
vertical meridian
Junctional rare

Optic
Let’s tractone of these exceptions now
address With few
exceptions,
LGN must be
Retrochiasmal Optic radiations
homonymous
hemianopia-like

Occipital cortex
144

Visual Field Defects


VF defect

Clinically Anything except


An elderly vasculopath presents c/o things ‘sneaking up obvious
on her from dzthe left.’ You check her CVFs—they’re
a vertical
Retina
fine. You get a 24-2—WNL OU. You send her on her way with reassurances that everything’s fine.
Clinically subtle dz
weeks later she’s on your schedule again with the same complaint. Just to be sure you repeat thechance)
meridian
Two cut
(unless by pure
VF, but
with the rarely-used 30-2 protocol—again, WNL. Reassure, discharge. Back
Nasal stepthe next week. Sigh. This
visit, for the first time in your career, you order Depressions
the never-used 60-2 Altitudinal
protocol—again, nothing. YOU’RE
FINE, YOU CRAZY OLD BAT! you yell at her. (Not really.) To placate her, youwedgeTemporal refer her to a neuro-oph,
Anything except
Optic nerve
who…Sends you a consult note detailing both her VF loss and the Arcuate location of the CNS changes a(dx: vertical
meridian cut
ischemic CVA) that produced it. What did you
Forget miss?
Scotomas
all of these specificCentralVF findings (unless by pure
You missed a classic case of loss of the fortemporal crescent . The
just a minute…In the temporal visual field of the eye chance)
Ceco-central
most general ipsilateral
to the field in question extends much farther
of terms,(~ 100 o
what ) that
candoes
we the
saycontribution
about VF from the fellow eye (~
60 ). Thus, there is a roughly 40 crescent
o o
in the
defects ipsilateral eye
associated withthat has noincorresponding contribution
lesions
from the fellow eye—it is hemianopia-like, each it Bitemporal
is
ofnot homonymous.
these locations? No commercially-available automated VF
hemianopia
analyzer is capable of detecting a temporal crescent; the only technology that can is Goldmann With few
Binasal are hemianopia
exceptions, will
Optic chiasm
perimetry. Lesions of the anterior occipital cortex responsible for this finding.
Junctional common
not cross the
vertical meridian
Junctional rare

Optic
Let’s tractone of these exceptions now
address With few
exceptions,
LGN must be
Retrochiasmal Optic radiations
homonymous
hemianopia-like

Occipital cortex
145

Visual Field Defects


VF defect

Clinically Anything except


An elderly vasculopath presents c/o things ‘sneaking up obvious
on her from dzthe left.’ You check her CVFs—they’re
a vertical
Retina
fine. You get a 24-2—WNL OU. You send her on her way with reassurances that everything’s fine.
Clinically subtle dz
weeks later she’s on your schedule again with the same complaint. Just to be sure you repeat thechance)
meridian
Two cut
(unless by pure
VF, but
with the rarely-used 30-2 protocol—again, WNL. Reassure, discharge. NasalBack
stepthe next week. Sigh. This
visit, for the first time in your career, you order Depressions
the never-used 60-2 Altitudinal
protocol—again, nothing. YOU’RE
FINE, YOU CRAZY OLD BAT! you yell at her. (Not really.) To placate her, youwedgeTemporal refer her to a neuro-oph,
Anything except
Optic nerve
who…Sends you a consult note detailing both her VF loss and the Arcuate location of the CNS changes a(dx: vertical
meridian cut
ischemic CVA) that produced it. What did you
Forget miss?
Scotomas
all of these specificCentralVF findings (unless by pure
You missed a classic case of loss of the fortemporal crescent . The
just a minute…In the temporal visual field of the eye chance)
Ceco-central
most general ipsilateral
to the field in question extends much farther
of terms,(~ 100 o
what ) that
candoes
we the
saycontribution
about VF from the fellow eye (~
60 ). Thus, there is a roughly 40 crescent
o o
in the
defects ipsilateral eye
associated withthat has noincorresponding contribution
lesions
from the fellow eye—it is hemianopia-like, each it Bitemporal
is
ofnot homonymous.
these locations? No commercially-available automated VF
hemianopia
analyzer is capable of detecting a temporal crescent; the only technology that can is Goldmann With few
Binasal are hemianopia
exceptions, will
Optic chiasm
perimetry. Lesions of the anterior occipital cortex responsible for this finding.
Junctional common
not cross the
vertical meridian
Junctional rare

Optic
Let’s tractone of these exceptions now
address With few
exceptions,
LGN must be
Retrochiasmal Optic radiations
homonymous
hemianopia-like

Occipital cortex
146

Visual Field Defects


VF defect

Clinically Anything except


An elderly vasculopath presents c/o things ‘sneaking up obvious
on her from dzthe left.’ You check her CVFs—they’re
a vertical
Retina
fine. You get a 24-2—WNL OU. You send her on her way with reassurances that everything’s fine.
Clinically subtle dz
weeks later she’s on your schedule again with the same complaint. Just to be sure you repeat thechance)
meridian
Two cut
(unless by pure
VF, but
with the rarely-used 30-2 protocol—again, WNL. Reassure, discharge. NasalBack
stepthe next week. Sigh. This
visit, for the first time in your career, you order Depressions
the never-used 60-2 Altitudinal
protocol—again, nothing. YOU’RE
FINE, YOU CRAZY OLD BAT! you yell at her. (Not really.) To placate her, youwedgeTemporal refer her to a neuro-oph,
Anything except
Optic nerve
who… Sends you a consult note detailing both her VF loss and theArcuate location of the CNS changesa(dx: vertical
meridian cut
ischemic CVA) that produced it. What did you
Forget miss?
Scotomas
all of these specificCentralVF findings (unless by pure
You missed a classic case of loss of the fortemporal crescent . The
just a minute…In the temporal visual field of the eye chance)
Ceco-central
most general ipsilateral
to the field in question extends much farther
of terms,(~ 100 o
what ) that
candoes
we the
saycontribution
about VF from the fellow eye (~
60 ). Thus, there is a roughly 40 crescent
o o
in the
defects ipsilateral eye
associated withthat has noincorresponding contribution
lesions
from the fellow eye—it is hemianopia-like, each it Bitemporal
is
ofnot homonymous.
these locations? No commercially-available automated VF
hemianopia
analyzer is capable of detecting a temporal crescent; the only technology that can is Goldmann With few
Binasal are hemianopia
exceptions, will
Optic chiasm
perimetry. Lesions of the anterior occipital cortex responsible for this finding.
Junctional common
not cross the
vertical meridian
Junctional rare

Optic
Let’s tractone of these exceptions now
address With few
exceptions,
LGN must be
Retrochiasmal Optic radiations
homonymous
hemianopia-like

Occipital cortex
147

Visual Field Defects


VF defect

Clinically Anything except


An elderly vasculopath presents c/o things ‘sneaking up obvious
on her from dzthe left.’ You check her CVFs—they’re
a vertical
Retina
fine. You get a 24-2—WNL OU. You send her on her way with reassurances that everything’s fine.
Clinically subtle dz
weeks later she’s on your schedule again with the same complaint. Just to be sure you repeat thechance)
meridian
Two cut
(unless by pure
VF, but
with the rarely-used 30-2 protocol—again, WNL. Reassure, discharge. NasalBack
stepthe next week. Sigh. This
visit, for the first time in your career, you order Depressions
the never-used 60-2 Altitudinal
protocol—again, nothing. YOU’RE
FINE, YOU CRAZY OLD BAT! you yell at her. (Not really.) To placate her, youwedgeTemporal refer her to a neuro-oph,
Anything except
Optic nerve
who… Sends you a consult note detailing both her VF loss and theArcuate location of the CNS changesa(dx: vertical
meridian cut
ischemic CVA) that produced it. What did you
Forget miss?
Scotomas
all of these specificCentralVF findings (unless by pure
You missed a classic case of loss of the fortemporal crescent . The
just a minute…In the temporal visual field of the eye chance)
Ceco-central
most general ipsilateral
to the field in question extends much farther
of terms,(~ 100 o
what ) that
candoes
we the
saycontribution
about VF from the fellow eye (~
60 ). Thus, there is a roughly 40 crescent
o o
in the
defects ipsilateral eye
associated withthat has noincorresponding contribution
lesions
from the fellow eye—it is hemianopia-like, each it Bitemporal
is
ofnot homonymous.
these locations? No commercially-available automated VF
hemianopia
analyzer is capable of detecting a temporal crescent; the only technology that can is Goldmann With few
Binasal are hemianopia
exceptions, will
Optic chiasm
perimetry. Lesions of the anterior occipital cortex responsible for this finding.
Junctional common
not cross the
vertical meridian
Junctional rare

Optic
Let’s tractone of these exceptions now
address With few
exceptions,
LGN must be
Retrochiasmal Optic radiations
homonymous
hemianopia-like

Occipital cortex
148

Visual Field Defects


VF defect

Clinically Anything except


An elderly vasculopath presents c/o things ‘sneaking up obvious
on her fromdzthe left.’ You check her CVFs—they’re
a vertical
Retina
fine. You get a 24-2—WNL OU. You send her on her way with reassurances that everything’s fine.
Clinically subtle dz
weeks later she’s on your schedule again with the same complaint. Just to be sure you repeat thechance)
meridian
Two cut
(unless by pure
VF, but
with the rarely-used 30-2 protocol—again, WNL. Reassure, discharge. NasalBack
stepthe next week. Sigh. This
visit, for the first time in your career, you order Depressions
the never-used 60-2 Altitudinal
protocol—again, nothing. YOU’RE
FINE, YOU CRAZY OLD BAT! you yell at her. (Not really.) To placate her, youwedge Temporal refer her to a neuro-oph,
Anything except
Optic nerve
who… Sends you a consult note detailing both her VF loss and theArcuate location of the CNS changesa(dx: vertical
meridian cut
ischemic CVA) that produced it. What did you
Forget miss?
Scotomas
all of these specificCentral VF findings (unless by pure
You missed a classic case of loss of the fortemporal crescent . The
just a minute…In
two words
the temporal visual field of the eye chance)
Ceco-central
most general ipsilateral
to the field in question extends much farther
of terms,(~ 100 o
what ) that
candoes
we the
saycontribution
about VF from the fellow eye (~
60 ). Thus, there is a roughly 40 crescent
o o
in the
defects ipsilateral eye
associated withthat has noincorresponding contribution
lesions
from the fellow eye—it is hemianopia-like, each it Bitemporal
is
ofnot
thesehomonymous.
locations? No commercially-available automated VF
hemianopia
analyzer is capable of detecting a temporal crescent; the only technology that can is Goldmann With few
Binasal are hemianopia
exceptions, will
Optic chiasm
perimetry. Lesions of the anterior occipital cortex responsible for this finding.
Junctional common
not cross the
vertical meridian
Junctional rare

Optic
Let’s tractone of these exceptions now
address With few
exceptions,
LGN must be
Retrochiasmal Optic radiations
homonymous
hemianopia-like

Occipital cortex
149

Visual Field Defects


VF defect

Clinically Anything except


An elderly vasculopath presents c/o things ‘sneaking up obvious
on her fromdzthe left.’ You check her CVFs—they’re
a vertical
Retina
fine. You get a 24-2—WNL OU. You send her on her way with reassurances that everything’s fine.
Clinically subtle dz
weeks later she’s on your schedule again with the same complaint. Just to be sure you repeat thechance)
meridian
Two cut
(unless by pure
VF, but
with the rarely-used 30-2 protocol—again, WNL. Reassure, discharge. NasalBack
stepthe next week. Sigh. This
visit, for the first time in your career, you order Depressions
the never-used 60-2 Altitudinal
protocol—again, nothing. YOU’RE
FINE, YOU CRAZY OLD BAT! you yell at her. (Not really.) To placate her, youwedgeTemporal refer her to a neuro-oph,
Anything except
Optic nerve
who… Sends you a consult note detailing both her VF loss and theArcuate location of the CNS changesa(dx: vertical
meridian cut
ischemic CVA) that produced it. What did you
Forget miss?
Scotomas
all of these specificCentralVF findings (unless by pure
You missed a classic case of loss of the fortemporal crescent . The
just a minute…In the temporal visual field of the eye chance)
Ceco-central
most general ipsilateral
to the field in question extends much farther
of terms,(~ 100 o
what ) that
candoes
we the
saycontribution
about VF from the fellow eye (~
60 ). Thus, there is a roughly 40 crescent
o o
in the
defects ipsilateral eye
associated withthat has noincorresponding contribution
lesions
from the fellow eye—it is hemianopia-like, each it Bitemporal
is
ofnot homonymous.
these locations? No commercially-available automated VF
hemianopia
analyzer is capable of detecting a temporal crescent; the only technology that can is Goldmann With few
Binasal are hemianopia
exceptions, will
Optic chiasm
perimetry. Lesions of the anterior occipital cortex responsible for this finding.
Junctional common
not cross the
vertical meridian
Junctional rare

Optic
Let’s tractone of these exceptions now
address With few
exceptions,
LGN must be
Retrochiasmal Optic radiations
homonymous
hemianopia-like

Occipital cortex
150

Visual Field Defects


VF defect

Clinically Anything except


An elderly vasculopath presents c/o things ‘sneaking up obvious
on her fromdzthe left.’ You check her CVFs—they’re
a vertical
Retina
fine. You get a 24-2—WNL OU. You send her on her way with reassurances that everything’s fine.
Clinically subtle dz
weeks later she’s on your schedule again with the same complaint. Just to be sure you repeat thechance)
meridian
Two cut
(unless by pure
VF, but
with the rarely-used 30-2 protocol—again, WNL. Reassure, discharge. Back
Nasal stepthe next week. Sigh. This
visit, for the first time in your career, you order Depressions
the never-used 60-2 Altitudinal
protocol—again, nothing. YOU’RE
FINE, YOU CRAZY OLD BAT! you yell at her. (Not really.) To placate her, youwedgeTemporal refer her to a neuro-oph,
Anything except
Optic nerve
who… Sends you a consult note detailing both her VF loss and theArcuate location of the CNS changesa(dx: vertical
meridian cut
ischemic CVA) that produced it. What did you
Forget miss?
Scotomas
all of these specificCentral
VF findings (unless by pure
You missed a classic case of loss of the fortemporal crescent . The
just a minute…In the temporal visual field of the eye chance)
Ceco-central
most general ipsilateral
to the field in question extends much farther
of terms,(~ 100
deg o
what ) than
candoes the contribution
we say about VF from the fellow eye (~deg
60 ). Thus, there is a roughly 40 crescent
o o
in theassociated
defects ipsilateral eye that
with has noin
lesions corresponding contribution
from the fellow eye—it is hemianopia-like, each it Bitemporal
is
ofnot homonymous.
these locations? No commercially-available automated VF
hemianopia
analyzer is capable of detecting a temporal crescent; the only technology that can is Goldmann With few
Binasal are hemianopia
exceptions, will
Optic chiasm
perimetry. Lesions of the anterior occipital cortex responsible for this finding.
Junctional common
not cross the
vertical meridian
Junctional rare

Optic
Let’s tractone of these exceptions now
address With few
exceptions,
LGN must be
Retrochiasmal Optic radiations
homonymous
hemianopia-like

Occipital cortex
151

Visual Field Defects


VF defect

Clinically Anything except


An elderly vasculopath presents c/o things ‘sneaking up obvious
on her fromdzthe left.’ You check her CVFs—they’re
a vertical
Retina
fine. You get a 24-2—WNL OU. You send her on her way with reassurances that everything’s fine.
Clinically subtle dz
weeks later she’s on your schedule again with the same complaint. Just to be sure you repeat thechance)
meridian
Two cut
(unless by pure
VF, but
with the rarely-used 30-2 protocol—again, WNL. Reassure, discharge. Back
Nasal stepthe next week. Sigh. This
visit, for the first time in your career, you order Depressions
the never-used 60-2 Altitudinal
protocol—again, nothing. YOU’RE
FINE, YOU CRAZY OLD BAT! you yell at her. (Not really.) To placate her, youwedgeTemporal refer her to a neuro-oph,
Anything except
Optic nerve
who… Sends you a consult note detailing both her VF loss and theArcuate location of the CNS changesa(dx: vertical
meridian cut
ischemic CVA) that produced it. What did you
Forget miss?
Scotomas
all of these specificCentral
VF findings (unless by pure
You missed a classic case of loss of the fortemporal crescent . The
just a minute…In the temporal visual field of the eye chance)
Ceco-central
most general ipsilateral
to the field in question extends much farther
of terms,(~ 100 o
what ) than
candoes the contribution
we say about VF from the fellow eye (~
60 ). Thus, there is a roughly 40 crescent
o o
in theassociated
defects ipsilateral eye that
with has noin
lesions corresponding contribution
from the fellow eye—it is hemianopia-like, each it Bitemporal
is
ofnot homonymous.
these locations? No commercially-available automated VF
hemianopia
analyzer is capable of detecting a temporal crescent; the only technology that can is Goldmann With few
Binasal are hemianopia
exceptions, will
Optic chiasm
perimetry. Lesions of the anterior occipital cortex responsible for this finding.
Junctional common
not cross the
vertical meridian
Junctional rare

Optic
Let’s tractone of these exceptions now
address With few
exceptions,
LGN must be
Retrochiasmal Optic radiations
homonymous
hemianopia-like

Occipital cortex
152

Visual Field Defects


VF defect

Clinically Anything except


An elderly vasculopath presents c/o things ‘sneaking up obvious
on her fromdzthe left.’ You check her CVFs—they’re
a vertical
Retina
fine. You get a 24-2—WNL OU. You send her on her way with reassurances that everything’s fine.
Clinically subtle dz
weeks later she’s on your schedule again with the same complaint. Just to be sure you repeat thechance)
meridian
Two cut
(unless by pure
VF, but
with the rarely-used 30-2 protocol—again, WNL. Reassure, discharge. Back
Nasal stepthe next week. Sigh. This
visit, for the first time in your career, you orderDepressions
the never-used 60-2 Altitudinal
protocol—again, nothing. YOU’RE
FINE, YOU CRAZY OLD BAT! you yell at her. (Not really.) To placate her, youwedge
Temporal refer her to a neuro-oph,
Anything except
Optic nerve
who… Sends you a consult note detailing both her VF loss and theArcuate location of the CNS changesa(dx: vertical
meridian cut
ischemic CVA) that produced it. What did you
Forget miss?
Scotomas
all of these specificCentral
VF findings (unless by pure
You missed a classic case of loss of the fortemporal crescent . The
just a minute…In the temporal visual field of the eye chance)
Ceco-central
most general ipsilateral
to the field in question extends much farther (~ 100
of terms,
o
what ) than
candoes the contribution
we say about VF from the fellow eye (~
60 ). Thus, there is a roughly 40 crescent
o o
in theassociated
defects ipsilateral eye that
with has noin
lesions corresponding contribution
from the fellow eye—it is hemianopia-like, each but
ofnot homonymous.
Bitemporal
these No commercially-available automated VF
hemianopia
locations?
analyzer is capable of detecting a temporal crescent; the only technology that can is Goldmann With few
Binasal are hemianopia
exceptions, will
Optic chiasm
perimetry. Lesions of the anterior occipital cortex responsible for this finding.
Junctional common
not cross the
vertical meridian
Junctional rare

Optic
Let’s tractone of these exceptions now
address With few
exceptions,
LGN must be
Retrochiasmal Optic radiations
homonymous
hemianopia-like

Occipital cortex
153

Visual Field Defects

Diagram of the nasal VF (60 degrees) and temporal VF (90-100 degrees).


The temporal 60-90o region is the temporal crescent.
154

Visual Field Defects


VF defect

Clinically Anything except


An elderly vasculopath presents c/o things ‘sneaking up obvious
on her fromdzthe left.’ You check her CVFs—they’re
a vertical
Retina
fine. You get a 24-2—WNL OU. You send her on her way with reassurances that everything’s fine.
Clinically subtle dz
weeks later she’s on your schedule again with the same complaint. Just to be sure you repeat thechance)
meridian
Two cut
(unless by pure
VF, but
with the rarely-used 30-2 protocol—again, WNL. Reassure, discharge. Back
Nasal stepthe next week. Sigh. This
visit, for the first time in your career, you orderDepressions
the never-used 60-2 Altitudinal
protocol—again, nothing. YOU’RE
FINE, YOU CRAZY OLD BAT! you yell at her. (Not really.) To placate her, youwedge
Temporal refer her to a neuro-oph,
Anything except
Optic nerve
who… Sends you a consult note detailing both her VF loss and theArcuate location of the CNS changesa(dx: vertical
meridian cut
ischemic CVA) that produced it. What did you
Forget miss?
Scotomas
all of these specificCentral
VF findings (unless by pure
You missed a classic case of loss of the fortemporal crescent . The
just a minute…In the temporal visual field of the eye chance)
Ceco-central
most general ipsilateral
to the field in question extends much farther (~ 100
of terms,
o
what ) than
candoes the contribution
we say about VF from the fellow eye (~
60 ). Thus, there is a roughly 40 crescent
o o
in theassociated
defects ipsilateral eye that
with has noin
lesions corresponding contribution
from the fellow eye—it is hemianopia-like, each but
ofnot homonymous.
Bitemporal
these No commercially-available automated VF
hemianopia
locations?
analyzer is capable of detecting a temporal crescent; the only technology that can is Goldmann With few
Binasal are hemianopia
exceptions, will
Optic chiasm
perimetry. Lesions of the anterior occipital cortex responsible for this finding.
Junctional common
not cross the
vertical meridian
Junctional rare

Optic
Let’s tractone of these exceptions now
address With few
exceptions,
LGN must be
Retrochiasmal Optic radiations
homonymous
hemianopia-like

Occipital cortex
155

Visual Field Defects


VF defect

Clinically Anything except


An elderly vasculopath presents c/o things ‘sneaking up obvious
on her fromdzthe left.’ You check her CVFs—they’re
a vertical
Retina
fine. You get a 24-2—WNL OU. You send her on her way with reassurances that everything’s fine.
Clinically subtle dz
weeks later she’s on your schedule again with the same complaint. Just to be sure you repeat thechance)
meridian
Two cut
(unless by pure
VF, but
with the rarely-used 30-2 protocol—again, WNL. Reassure, discharge. Back
Nasal stepthe next week. Sigh. This
visit, for the first time in your career, you orderDepressions
the never-used 60-2 Altitudinal
protocol—again, nothing. YOU’RE
FINE, YOU CRAZY OLD BAT! you yell at her. (Not really.) To placate her, youwedge
Temporal refer her to a neuro-oph,
Anything except
Optic nerve
who… Sends you a consult note detailing both her VF loss and theArcuate location of the CNS changesa(dx: vertical
meridian cut
ischemic CVA) that produced it. What did you
Forget miss?
Scotomas
all of these specificCentral
VF findings (unless by pure
You missed a classic case of loss of the fortemporal crescent . The
just a minute…In the temporal visual field of the eye chance)
Ceco-central
most general ipsilateral
to the field in question extends much farther (~ 100
of terms,
o
what ) than
candoes the contribution
we say about VF from the fellow eye (~
60 ). Thus, there is a roughly 40 crescent
o o
in theassociated
defects ipsilateral eye that
with has noin
lesions corresponding contribution
from the fellow eye—it is hemianopia-like, each but
ofnot homonymous.
Bitemporal
these No commercially-available automated VF
hemianopia
locations?
analyzer is capable of detecting a temporal crescent; the only technology that can is Goldmann With few
Binasal are hemianopia
exceptions, will
Optic chiasm
perimetry. Lesions of the anterior occipital cortex responsible for this finding.
Junctional common
not cross the
vertical meridian
Junctional rare

Optic
Let’s tractone of these exceptions now
address With few
exceptions,
LGN must be
Retrochiasmal Optic radiations
homonymous
hemianopia-like

Occipital cortex
156

Visual Field Defects


VF defect

Clinically Anything except


An elderly vasculopath presents c/o things ‘sneaking up obvious
on her fromdzthe left.’ You check her CVFs—they’re
a vertical
Retina
fine. You get a 24-2—WNL OU. You send her on her way with reassurances that everything’s fine.
Clinically subtle dz
weeks later she’s on your schedule again with the same complaint. Just to be sure you repeat thechance)
meridian
Two cut
(unless by pure
VF, but
with the rarely-used 30-2 protocol—again, WNL. Reassure, discharge. Back
Nasal stepthe next week. Sigh. This
visit, for the first time in your career, you orderDepressions
the never-used 60-2 Altitudinal
protocol—again, nothing. YOU’RE
FINE, YOU CRAZY OLD BAT! you yell at her. (Not really.) To placate her, youwedge
Temporal refer her to a neuro-oph,
Anything except
Optic nerve
who… Sends you a consult note detailing both her VF loss and theArcuate location of the CNS changesa(dx: vertical
meridian cut
ischemic CVA) that produced it. What did you
Forget miss?
Scotomas
all of these specificCentral
VF findings (unless by pure
You missed a classic case of loss of the fortemporal crescent . The
just a minute…In the temporal visual field of the eye chance)
Ceco-central
most general ipsilateral
to the field in question extends much farther (~ 100
of terms,
o
what ) than
candoes the contribution
we say about VF from the fellow eye (~
60 ). Thus, there is a roughly 40 crescent
o o
in theassociated
defects ipsilateral eye that
with has noin
lesions corresponding contribution
from the fellow eye—it is hemianopia-like, each but
ofnot homonymous.
Bitemporal
these No commercially-available automated VF
hemianopia
locations?
analyzer is capable of detecting a temporal crescent; the only technology that can is Goldmann With few
Binasal are hemianopia
exceptions, will
Optic chiasm
perimetry. Lesions of the anterior occipital cortex
anterior vs
posterior responsible for this finding.
Junctional common
not cross the
vertical meridian
Junctional rare

Optic
Let’s tractone of these exceptions now
address With few
exceptions,
LGN must be
Retrochiasmal Optic radiations
homonymous
hemianopia-like

Occipital cortex
157

Visual Field Defects


VF defect

Clinically Anything except


An elderly vasculopath presents c/o things ‘sneaking up obvious
on her fromdzthe left.’ You check her CVFs—they’re
a vertical
Retina
fine. You get a 24-2—WNL OU. You send her on her way with reassurances that everything’s fine.
Clinically subtle dz
weeks later she’s on your schedule again with the same complaint. Just to be sure you repeat thechance)
meridian
Two cut
(unless by pure
VF, but
with the rarely-used 30-2 protocol—again, WNL. Reassure, discharge. Back
Nasal stepthe next week. Sigh. This
visit, for the first time in your career, you orderDepressions
the never-used 60-2 Altitudinal
protocol—again, nothing. YOU’RE
FINE, YOU CRAZY OLD BAT! you yell at her. (Not really.) To placate her, youwedge
Temporal refer her to a neuro-oph,
Anything except
Optic nerve
who… Sends you a consult note detailing both her VF loss and theArcuate location of the CNS changesa(dx: vertical
meridian cut
ischemic CVA) that produced it. What did you
Forget miss?
Scotomas
all of these specificCentral
VF findings (unless by pure
You missed a classic case of loss of the fortemporal crescent . The
just a minute…In the temporal visual field of the eye chance)
Ceco-central
most general ipsilateral
to the field in question extends much farther (~ 100
of terms,
o
what ) than
candoes the contribution
we say about VF from the fellow eye (~
60 ). Thus, there is a roughly 40 crescent
o o
in theassociated
defects ipsilateral eye that
with has noin
lesions corresponding contribution
from the fellow eye—it is hemianopia-like, each but
ofnot homonymous.
Bitemporal
these No commercially-available automated VF
hemianopia
locations?
analyzer is capable of detecting a temporal crescent; the only technology that can is Goldmann With few
Binasal are hemianopia
exceptions, will
Optic chiasm
perimetry. Lesions of the anterior occipital cortex responsible for this finding.
Junctional common
not cross the
vertical meridian
Junctional rare

Optic
Let’s tractone of these exceptions now
address With few
exceptions,
LGN must be
Retrochiasmal Optic radiations
homonymous
hemianopia-like

Occipital cortex
158

Visual Field Defects

Images showcasing the location of a lesion producing Temporal Crescent Syndrome


159

 Whichof the following is not associated with


bitemporal visual-field loss?
 Sectoral RP
 Glaucoma
 Fuchs coloboma
 Chiasmal lesion
 Toxic/hereditary/nutritional optic neuropathy
160

Q/A
 Which of the following is not associated with bitemporal visual-field loss?
 Sectoral RP
 Glaucoma
 Fuchs coloboma
 Chiasmal lesion
 Toxic/hereditary/nutritional optic neuropathy

 Glaucoma. Hemianopic (= respects the vertical midline) bitemporal VF


loss is associated exclusively with lesions compressing the chiasm,
specifically the mid-chiasm .
mid- vs lateral chiasm
161

A
 Which of the following is not associated with bitemporal visual-field loss?
 Sectoral RP
 Glaucoma
 Fuchs coloboma
 Chiasmal lesion
 Toxic/hereditary/nutritional optic neuropathy

 Glaucoma. Hemianopic (= respects the vertical midline) bitemporal VF


loss is associated exclusively with lesions compressing the chiasm,
specifically the mid-chiasm .
162

A
 Which of the following is not associated with bitemporal visual-field loss?
 Sectoral RP
 Glaucoma
 Fuchs coloboma
 Chiasmal lesion
 Toxic/hereditary/nutritional optic neuropathy

 Glaucoma. Hemianopic (= respects the vertical midline) bitemporal VF


loss is associated exclusively with lesions compressing the chiasm,
specifically the mid-chiasm . Other causes of bitemporal loss do not
respect the midline (except by happenstance). Sectoral RP is
symmetric bilaterally, and thus can affect the temporal VF bilaterally.
163

Images from JP Marques et al, EYS-Associated


Sector Retinitis Pigmentosa. Graefe’s Archives
Sectoral RP for Clinical and Experimental Ophthalmology,
2022 Apr;260(4):1405-1413.
With kind permission of the first author.
164

A
 Which of the following is not associated with bitemporal visual-field loss?
 Sectoral RP
 Glaucoma
 Fuchs coloboma
 Chiasmal lesion
 Toxic/hereditary/nutritional optic neuropathy

 Glaucoma. Hemianopic (= respects the vertical midline) bitemporal VF


loss is associated exclusively with lesions compressing the chiasm,
specifically the mid-chiasm . Other causes of bitemporal loss do not
respect the midline (except by happenstance). Sectoral RP is
symmetric bilaterally, and thus can affect the temporal VF bilaterally.
Fuchs coloboma (aka tilted disc syndrome) is associated with
bitemporal loss that resolves with proper correction.
165

Tilted disc: Superior bitemporal VF defects


166

A
 Which of the following is not associated with bitemporal visual-field loss?
 Sectoral RP
 Glaucoma
 Fuchs coloboma
 Chiasmal lesion
 Toxic/hereditary/nutritional optic neuropathy

 Glaucoma. Hemianopic (= respects the vertical midline) bitemporal VF


loss is associated exclusively with lesions compressing the chiasm,
specifically the mid-chiasm . Other causes of bitemporal loss do not
respect the midline (except by happenstance). Sectoral RP is
symmetric bilaterally, and thus can affect the temporal VF bilaterally.
Fuchs coloboma (aka tilted disc syndrome) is associated with
bitemporal loss that resolves with proper correction.
Toxic/hereditary/nutritional optic neuropathy is associated with bilateral
cecocentral VF loss, which can mimic bitemporal loss.
167

Visual field defects characteristic of toxic and metabolic optic neuropathies


168

A
 Which of the following is not associated with bitemporal visual-field loss?
 Sectoral RP
 Glaucoma
 Fuchs coloboma
 Chiasmal lesion
 Toxic/hereditary/nutritional optic neuropathy

 Glaucoma. Hemianopic (= respects the vertical midline) bitemporal VF


loss is associated exclusively with lesions compressing the chiasm,
specifically the mid-chiasm . Other causes of bitemporal loss do not
respect the midline (except by happenstance). Sectoral RP is
symmetric bilaterally, and thus can affect the temporal VF bilaterally.
Fuchs coloboma (aka tilted disc syndrome) is associated with
bitemporal loss that resolves with proper correction.
Toxic/hereditary/nutritional optic neuropathy is associated with bilateral
cecocentral VF loss, which can mimic bitemporal loss. Glaucoma
almost always affects the nasal VF long before the temporal field is
involved—if anything, glaucoma is far more likely to cause binasal
VF loss (although this is a very rare occurrence).
169

Q
 Which of the following is not associated with bitemporal visual-field loss?
 Sectoral RP
 Glaucoma
 Fuchs coloboma
How on earth does a tilted disc produce a bitemporal VF defect, and how can the defect be
resolvedviaChiasmal
refraction? lesion
It’s actually pretty straightforward.
 Toxic/hereditary/nutritional optic neuropathy
The area including and adjacent to the inferior pole of a tilted disc is staphylomatous. This
means the ‘axial length’ of the photoreceptors within this region is greater than that of the rest of
 Glaucoma. Hemianopic
the posterior pole. Because of this(= respects
extra the
axial length, the vertical midline)
correction used during bitemporal
VF testing VF
loss
(whichis associated
is based exclusively
on the refraction with lesions compressing
of the non-staphylomatous fovea) is not myopic the chiasm,
enough for the
inferior peripapillary region. Because this region is out of focus, it will manifest a refractive
specifically the And
scotoma on the test. mid-chiasm. Other
because the retina causes
involved in this of bitemporal
scotoma losstodo
is inferonasal the not
respect the that
fovea, it follows midline (except
the resulting by happenstance).
VF defect will be superotemporal Sectoral RP as
to fixation. And, is Fuchs
coloboma is virtually always bilateral, these superotemporal VF defects are present bilaterally.
symmetric bilaterally, and thus can affect the temporal VF bilaterally.
Fuchs coloboma (aka tilted disc syndrome) is associated with
bitemporal loss that resolves with proper correction.
Toxic/hereditary/nutritional optic neuropathy is associated with bilateral
cecocentral VF loss, which can mimic bitemporal loss. Glaucoma
almost always affects the nasal VF long before the temporal field is
involved--if anything, glaucoma is far more likely to cause binasal
VF loss (although this is a very rare occurrence).
170

A
 Which of the following is not associated with bitemporal visual-field loss?
 Sectoral RP
 Glaucoma
 Fuchs coloboma
How on earth does a tilted disc produce a bitemporal VF defect, and how can the defect be
resolvedviaChiasmal
refraction? lesion
It’s actually pretty straightforward.
 Toxic/hereditary/nutritional optic neuropathy
The area including and adjacent to the inferior pole of a tilted disc is staphylomatous. This
means the ‘axial length’ of the photoreceptors within this region is greater than that of the rest of
 Glaucoma. Hemianopic
the posterior pole. Because of this(= respects
extra the
axial length, the vertical midline)
correction used during bitemporal
VF testing VF
loss
(whichis associated
is based exclusively
on the refraction with lesions compressing
of the non-staphylomatous fovea) is not myopic the chiasm,
enough for the
inferior peripapillary region. Because this region is out of focus, it will manifest a refractive
specifically the And
scotoma on the test. mid-chiasm. Other
because the retina causes
involved in this of bitemporal
scotoma losstodo
is inferonasal the not
respect the that
fovea, it follows midline (except
the resulting by happenstance).
VF defect will be superotemporal Sectoral RP as
to fixation. And, is Fuchs
coloboma is virtually always bilateral, these superotemporal VF defects are present bilaterally.
symmetric bilaterally, and thus can affect the temporal VF bilaterally.
Fuchs coloboma (aka tilted disc syndrome) is associated with
bitemporal loss that resolves with proper correction.
Toxic/hereditary/nutritional optic neuropathy is associated with bilateral
cecocentral VF loss, which can mimic bitemporal loss. Glaucoma
almost always affects the nasal VF long before the temporal field is
involved--if anything, glaucoma is far more likely to cause binasal
VF loss (although this is a very rare occurrence).
171

A
 Which of the following is not associated with bitemporal visual-field loss?
 Sectoral RP
 Glaucoma
 Fuchs coloboma
How on earth does a tilted disc produce a bitemporal VF defect, and how can the defect be
resolvedviaChiasmal
refraction? lesion
It’s actually pretty straightforward.
 Toxic/hereditary/nutritional optic neuropathy
The area including and adjacent to the inferior pole of a tilted disc is staphylomatous. This
means the ‘axial length’ of the photoreceptors within this region is greater than that of the rest of
 Glaucoma. Hemianopic
the posterior pole. Because of this(= respects
extra the
axial length, the vertical midline)
correction used during bitemporal
VF testing VF
loss
(whichis associated
is based exclusively
on the refraction with lesions compressing
of the non-staphylomatous fovea) is not myopic the chiasm,
enough for the
inferior peripapillary region. Because this region is out of focus, it will manifest a refractive
specifically the And
scotoma on the test. mid-chiasm. Other
because the retina causes
involved in this of bitemporal
scotoma losstodo
is inferonasal the not
respect the that
fovea, it follows midline (except
the resulting by happenstance).
VF defect will be superotemporal Sectoral
to fixation. RP
And, is
as Fuchs
coloboma is virtually always bilateral, these superotemporal VF defects are present bilaterally.
symmetric bilaterally, and thus can affect the temporal VF bilaterally.
Fuchs coloboma (aka tilted disc syndrome) is associated with
bitemporal loss that resolves with proper correction.
Toxic/hereditary/nutritional optic neuropathy is associated with bilateral
cecocentral VF loss, which can mimic bitemporal loss. Glaucoma
almost always affects the nasal VF long before the temporal field is
involved--if anything, glaucoma is far more likely to cause binasal
VF loss (although this is a very rare occurrence).
172

A
 Which of the following is not associated with bitemporal visual-field loss?
 Sectoral RP
 Glaucoma
 Fuchs coloboma
How on earth does a tilted disc produce a bitemporal VF defect, and how can the defect be
resolvedviaChiasmal
refraction? lesion
It’s actually pretty straightforward.
 Toxic/hereditary/nutritional optic neuropathy
The area including and adjacent to the inferior pole of a tilted disc is staphylomatous. This
means the ‘axial length’ of the photoreceptors within this region is greater than that of the rest of
 Glaucoma. Hemianopic
the posterior pole. Because of this(= respects
extra the
axial length, the vertical midline)
correction used during bitemporal
VF testing VF
loss
(whichis associated
is based exclusively
on the refraction with lesions compressing
of the non-staphylomatous fovea) is not myopic the chiasm,
enough for the
inferior peripapillary region. Because this region is out of focus, it will manifest a refractive
specifically the And
scotoma on the test. mid-chiasm. Other
because the retina causes
involved in this of bitemporal
scotoma losstodo
is inferonasal the not
respect the that
fovea, it follows midline (except
the resulting by happenstance).
VF defect will be superotemporal Sectoral
to fixation. RP
And, is
as Fuchs
coloboma is virtually always bilateral, these superotemporal VF defects are present bilaterally.
symmetric bilaterally, and thus can affect the temporal VF bilaterally.
Fuchs coloboma (aka tilted disc syndrome) is associated with
bitemporal loss that resolves with proper correction.
Toxic/hereditary/nutritional optic neuropathy is associated with bilateral
cecocentral VF loss, which can mimic bitemporal loss. Glaucoma
almost always affects the nasal VF long before the temporal field is
involved--if anything, glaucoma is far more likely to cause binasal
VF loss (although this is a very rare occurrence).

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