Understanding Visual Field Defects
Understanding Visual Field Defects
? ?
Here is a representation of the VF for each eye. Which is OD, and which OS?
2
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
? ?
? ? ? ?
? ?
OS OD
Measured in degrees from fixation, how far does the normal VF extend
superiorly, inferiorly, nasally and temporally?
4
60o 60o
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
? ?
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
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
? ?
OS OD
How far in degrees from fixation is the blind spot?
8
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
most anterior
Retina
location
Retina
Optic nerve
next location
Retina
Optic nerve
Optic
next chiasm
location
12
Retina
Optic nerve
Optic chiasm
Retina
Optic nerve
Optic chiasm
Retrochiasmal
14
Clinically obvious
two very general dz
Retina categories of retinal dz
Clinically subtle dz
Optic nerve
Optic chiasm
Retrochiasmal
15
Clinically obvious dz
Retina Clinically subtle dz
Optic nerve
Optic chiasm
Retrochiasmal
16
Clinically obvious dz
Retina Clinically subtle dz
What is meant by clinically obvious vs clinically subtle retinal dz?
Optic nerve
Optic chiasm
Retrochiasmal
17
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
Optic chiasm
Retrochiasmal
19
Optic chiasm
Retrochiasmal
20
Optic chiasm
Retrochiasmal
21
Optic chiasm
Retrochiasmal
22
Clinically obvious dz
Retina Clinically subtle dz
Optic chiasm
Retrochiasmal
23
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
Most? Where will the others synapse, and what are they responsible for?
32
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
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
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
‘Most’? Where will the others synapse, and what are they responsible for?
The hypothalamus, where they are involved in modulating circadian responses
36
Clinically obvious dz
Retina Clinically subtle dz
Depressions
two general
Optic nerve categories of ON
VF defects
Scotomas
Optic chiasm
Retrochiasmal
37
Clinically obvious dz
Retina Clinically subtle dz
Depressions
Optic nerve
Scotomas
Optic chiasm
Retrochiasmal
38
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
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
Clinically obvious dz
Retina Clinically subtle dz
Nasal step
three specific
Depressions Altitudinal
depressions
Temporal wedge
Optic nerve
Scotomas
Optic chiasm
Retrochiasmal
41
Clinically obvious dz
Retina Clinically subtle dz
Nasal step
Depressions Altitudinal
Temporal wedge
Optic nerve
Scotomas
Optic chiasm
Retrochiasmal
42
Clinically obvious dz
Retina Clinically subtle dz
Nasal step
Depressions Altitudinal
Temporal wedge
Optic nerve
Scotomas
Superior nasal step
Optic chiasm
Retrochiasmal
43
Clinically obvious dz
Retina Clinically subtle dz
Nasal step
Depressions Altitudinal
Temporal wedge
Optic nerve
Scotomas
Superior altitudinal
Optic chiasm
Inferior altitudinal
Retrochiasmal
44
Clinically obvious dz
Retina Clinically subtle dz
Nasal step
Depressions Altitudinal
Temporal wedge
Optic nerve
Scotomas
Optic chiasm
Retrochiasmal
45
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
Clinically obvious dz
Retina Clinically subtle dz
Nasal step
Depressions Altitudinal
Temporal wedge
Optic nerve Arcuate
Scotomas Central
Ceco-central
Optic chiasm
Retrochiasmal
47
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
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
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
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
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
#1?
Optic nerve Arcuate fibers
#2?
#3?
Nasal fibers
head
Optic chiasm
1
Retrochiasmal
53
Papillomacular bundle
Optic nerve Arcuate fibers
#2?
#3?
Nasal fibers
head
Optic chiasm
Retrochiasmal
54
Papillomacular bundle
Optic nerve Arcuate fibers
#2?
#3?
Nasal fibers
head
Optic chiasm 2
Retrochiasmal
55
Papillomacular bundle
Optic nerve Arcuate fibers
#3?
Nasal fibers
head
Optic chiasm
Retrochiasmal
56
Papillomacular bundle
Optic nerve Arcuate fibers
#3?
Nasal fibers
head
Optic chiasm
3
Retrochiasmal
57
Papillomacular bundle
Optic nerve Arcuate fibers
Nasal radiating fibers
head
Optic chiasm
Retrochiasmal
58
Papillomacular bundle
Optic nerve Arcuate fibers
Nasal radiating fibers
head
Retrochiasmal
59
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
Optic chiasm
Retrochiasmal
60
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
Optic chiasm
Retrochiasmal
79
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
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
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
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
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
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
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
Optic chiasm
Retrochiasmal
92
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
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
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
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
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
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
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
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
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
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
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
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
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
(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
Optic chiasm
Binasal hemianopia
Junctional common
?
exceptions, will
not cross the
vertical meridian
Junctional rare
Retrochiasmal LGN
Optic radiations
?
exceptions, must
be homonymous
hemianopia-like
Occipital cortex
107
Optic chiasm
Binasal hemianopia
Junctional common
?
exceptions, will
not cross the
vertical meridian
Junctional rare
Retrochiasmal LGN
Optic radiations
?
exceptions, must
be homonymous
hemianopia-like
Occipital cortex
108
Optic chiasm
Binasal hemianopia
Junctional common
?
exceptions, will
not cross the
vertical meridian
Junctional rare
Retrochiasmal LGN
Optic radiations
?
exceptions, must
be homonymous
hemianopia-like
Occipital cortex
109
Optic chiasm
Binasal hemianopia
Junctional common
?
exceptions, will
not cross the
vertical meridian
Junctional rare
Retrochiasmal LGN
Optic radiations
?
exceptions, must
be homonymous
hemianopia-like
Occipital cortex
110
Retrochiasmal LGN
Optic radiations
?
exceptions, must
be homonymous
hemianopia-like
Occipital cortex
111
Retrochiasmal LGN
Optic radiations
?
exceptions, must
be homonymous
hemianopia-like
Occipital cortex
112
Occipital cortex
113
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
Clinically obvious dz
Retina Clinically subtle dz
Nasal step
Depressions Altitudinal
Temporal wedge
Optic nerve Arcuate
Scotomas Central
Ceco-central
Here’s why:
Temporal VF Temporal VF
The nasal retinas are responsible
for the temporal visual fields.
Here’s why:
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
Nasal VF Nasal VF
Here’s why:
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
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
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
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
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
Bitemporal hemianopia
Binasal hemianopia
Optic chiasm Junctional common
Junctional rare
Optic tract
LGN
Retrochiasmal Optic radiations
Occipital cortex
126
Bitemporal hemianopia
Binasal hemianopia
Optic chiasm Junctional common
Junctional rare
Optic tract
LGN
Retrochiasmal Optic radiations
Occipital cortex
127
Bitemporal hemianopia
Binasal hemianopia
Optic chiasm Junctional common
Junctional rare
Optic tract
LGN
Retrochiasmal Optic radiations
Occipital cortex
128
Bitemporal hemianopia
Binasal hemianopia
Optic chiasm Junctional common
Junctional rare
Optic tract
LGN
Retrochiasmal Optic radiations
Occipital cortex
129
Bitemporal hemianopia
Binasal hemianopia
Optic chiasm Junctional common
Junctional rare
Optic tract
LGN
Retrochiasmal Optic radiations
Occipital cortex
130
Bitemporal hemianopia
Binasal hemianopia
Optic chiasm Junctional common
Junctional rare
Optic tract
LGN
Retrochiasmal Optic radiations
Occipital cortex
131
Bitemporal hemianopia
Binasal hemianopia
Optic chiasm Junctional common
Junctional rare
Optic tract
LGN
Retrochiasmal Optic radiations
Occipital cortex
132
Bitemporal hemianopia
Binasal hemianopia
Optic chiasm Junctional common
Junctional rare
Optic tract
LGN
Retrochiasmal Optic radiations
Occipital cortex
133
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
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
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
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
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
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
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
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
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
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
Optic
Let’s tractone of these exceptions now
address With few
exceptions,
LGN must be
Retrochiasmal Optic radiations
homonymous
hemianopia-like
Occipital cortex
144
Optic
Let’s tractone of these exceptions now
address With few
exceptions,
LGN must be
Retrochiasmal Optic radiations
homonymous
hemianopia-like
Occipital cortex
145
Optic
Let’s tractone of these exceptions now
address With few
exceptions,
LGN must be
Retrochiasmal Optic radiations
homonymous
hemianopia-like
Occipital cortex
146
Optic
Let’s tractone of these exceptions now
address With few
exceptions,
LGN must be
Retrochiasmal Optic radiations
homonymous
hemianopia-like
Occipital cortex
147
Optic
Let’s tractone of these exceptions now
address With few
exceptions,
LGN must be
Retrochiasmal Optic radiations
homonymous
hemianopia-like
Occipital cortex
148
Optic
Let’s tractone of these exceptions now
address With few
exceptions,
LGN must be
Retrochiasmal Optic radiations
homonymous
hemianopia-like
Occipital cortex
149
Optic
Let’s tractone of these exceptions now
address With few
exceptions,
LGN must be
Retrochiasmal Optic radiations
homonymous
hemianopia-like
Occipital cortex
150
Optic
Let’s tractone of these exceptions now
address With few
exceptions,
LGN must be
Retrochiasmal Optic radiations
homonymous
hemianopia-like
Occipital cortex
151
Optic
Let’s tractone of these exceptions now
address With few
exceptions,
LGN must be
Retrochiasmal Optic radiations
homonymous
hemianopia-like
Occipital cortex
152
Optic
Let’s tractone of these exceptions now
address With few
exceptions,
LGN must be
Retrochiasmal Optic radiations
homonymous
hemianopia-like
Occipital cortex
153
Optic
Let’s tractone of these exceptions now
address With few
exceptions,
LGN must be
Retrochiasmal Optic radiations
homonymous
hemianopia-like
Occipital cortex
155
Optic
Let’s tractone of these exceptions now
address With few
exceptions,
LGN must be
Retrochiasmal Optic radiations
homonymous
hemianopia-like
Occipital cortex
156
Optic
Let’s tractone of these exceptions now
address With few
exceptions,
LGN must be
Retrochiasmal Optic radiations
homonymous
hemianopia-like
Occipital cortex
157
Optic
Let’s tractone of these exceptions now
address With few
exceptions,
LGN must be
Retrochiasmal Optic radiations
homonymous
hemianopia-like
Occipital cortex
158
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
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
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
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
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
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
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
resolvedviaChiasmal
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
resolvedviaChiasmal
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
resolvedviaChiasmal
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
resolvedviaChiasmal
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).