Professional Documents
Culture Documents
MATA
MODUL 5-2
Departemen Radiologi
Fakultas Kedokteran Universitas Diponegoro
Orbita
Intra-extraconal space
Modalitas Imejing
X Ray
- waters: inferior wall
- caldwell : superior dan lateral wall
- lateral : lateral wall
- rhese : foramen opticum
CT Scan
- Multiplanar CT, 3D rekonstruksi
- Anatomy and pathology bulbus oculi, soft tissue , orbital bones
MRI
- Multiplanar MRI
- Anatomy and pathology bulbus oculi ,soft tissue
Water view
Sinus
ethmoidales
anterior
Dinding
Sinus lateral
ethmoidales orbita
posterior
Dinding superior
sinus maksilaris
Dinding medial
sinus Sinus maksilaris
maksilaris
Caldwell view
Sinus frontalis
Sinus
frontalis
Lamina cribosa
Proc clinoideus
Sella turcica
RHESE/PARIETO-ORBITAL PROJ
⬜ - Both sides are generraly taken for comparison
⬜ - Erect or supine posisition
⬜ - Oblique ( rotate )head 37 0 of toward side of
interest. Rest patients chin, check and nose
against head unit or toble top
⬜ - Midsagital plane will from 53 o angle with
film
⬜ - Central ray perpendicular
RHESE/PARIETO-ORBITAL PROJ
MODIFIED PARETOACANTHIAL
PROJ /MODIFIED WATERS
METHODE
MODIFIED PARETOACANTHIAL
PROJ /MODIFIED WATERS
METHODE
Check List
⬜ Choice of Imaging modalities
⬜ Clinical history from patient
⬜ Prior alergy drugs or contrast agent
⬜ GFR (iodium and gadolinium contrast agent)
CT or MRI ???
• CT is the first-line imaging modality for orbital
evaluation in the acute setting, with MR imaging
playing an important secondary role in the diagnostic
work-up.
Need onsite injection contrast media in nasolacrimal duct for evaluating patency of
the duct
Infection
Inflammation
Inflammation
Inflammation
Vascular abnormalities
Fibrous Dysplasia
⬜ Fibrous dysplasia (FD) is a non-neoplastic
tumour-like congenital process, manifested as a
localised defect in osteoblastic differentiation
and maturation, with replacement of normal
bone with large fibrous stroma and islands
of immature woven bone. FD has a varied
radiographic appearance. If they are
asymptomatic, they do not require treatment.
Distribution
Polyostotic form
Monostotic form ⬜often unilateral and monomelic:
⬜ ribs: 28%, most common one limb
⬜ proximal femur: 23% ⬜femur: 91%
⬜ tibia ⬜tibia: 81%
⬜ craniofacial bones: 10-25% ⬜pelvis: 78%
⬜ humerus ⬜foot: 73%
⬜ribs
⬜skull and facial bones: 50%
⬜upper extremities
⬜lumbar spine: 14%
⬜clavicle: 10%
⬜cervical spine: 7%
Fibrous Dysplasia
Radiographic features
Plain film
⬜ground-glass matrix
⬜may be completely lucent (cystic) or sclerotic
⬜well circumscribed lesions
⬜no periosteal reaction
CT
⬜ground-glass opacities: 56%
⬜homogeneously sclerotic: 23%
⬜cystic: 21%
⬜well-defined borders
⬜expansion of the bone, with intact overlying bone
⬜endosteal scalloping may be seen
MRI
⬜MRI is not particularly useful in differentiating fibrous
dysplasia from other entities as there is marked variability
in the appearance of the bone lesions, and they can often
resemble a tumour or more aggressive lesions.
⬜T1: heterogeneous signal, usually intermediate
⬜T2: heterogeneous signal, usually low, but may have
regions of higher signal
⬜T1 C+ (Gd): heterogeneous contrast enhancement 4
Nuclear Medicine
⬜Demonstrates increased tracer uptake on Tc99 bone
scans (lesions remain metabolically active into adulthood).
Fibrous Dysplasia
MENINGIOMA
⬜ Meningiomas are extra-axial tumours are extra-axial tumours and represent the
most common tumour of the meninges are extra-axial tumours and represent the
most common tumour of the meninges. They are a non-glial neoplasm that
originates from the arachnoid cap cells of the meninges. They are typically benign
with a low recurrence rate but rarely can be malignant.
Clinical presentation
⬜ asymptomatic.
⬜ headache: 36%
⬜ paresis: 22%
⬜ change in mental status: 21%
⬜ focal neurological deficits
⬜ convexity/parasagittal: seizures and hemiparesis
⬜ basisphenoid: visual field defect
⬜ cavernous sinus: cranial nerve deficit(s)
⬜ frontal: anosmia (although often become very large before becoming symptomatic)
⬜ dural venous sinus invasion/dural venous sinus thrombosis
⬜ intraosseous extension: may be hyperostotic or osteolytic and may result in local
mass effect (e.g. proptosis)
Plain radiography
⬜Plain films no longer have a role in the diagnosis or management of
meningiomas. Historically a number of features were observed, including:
⬜enlarged meningeal artery grooves
⬜hyperostosis or lytic regions
⬜Calcification
CT
⬜60% slightly hyperdense to normal brain, the rest are more isodense
⬜20-30% have some calcification 8
⬜72% brightly and homogeneously contrast enhance 8, less frequent in
malignant or cystic variants
⬜hyperostosis
◼ typical for meningiomas that abut the base of the skull
◼ need to distinguish reactive hyperostosis from skull vault invasion
(eventually involves the outer table too)
⬜lytic regions: particularly in higher grade lesions
⬜pneumosinus dilatans
MRI
As is the case with most other intracranial pathology, MRI is the investigation of
choice for the diagnosis and characterisation of meningiomas. When
appearance and location is typical, the diagnosis can be made with a very high
degree of certainty. In many instances however the appearances are atypical.
Meningiomas typically appear as extra-axial masses with a broad dural base.
They are usually homogeneous and well circumscribed, although many
variants are encountered.
Signal characteristics include:
T1
isointense: ~60-90%
somewhat hypointense: 10-40% compared to grey matter
T1 C+ (Gd): usually intense and homogeneous enhancement
T2
isointense: ~50%
hyperintense: 35-40%
usually correlates with soft textures and hypervascular tumours
DWI: atypical and malignant subtypes may show greater than expected
restricted diffusion although recent work suggests that this is not useful in
prospectively predicting histological grade
MR spectroscopy
MR perfusion
MENINGIOMA
PSEUDO TUMOR
⬜ Orbital pseudotumour is an idiopathic
inflammatory condition that usually involves
the extraocular muscles although, in some
cases there is inflammatory change involving
the uvea, sclera, lacrimal gland and retrobulbar
soft tissues. The exact aetiology is not known.
Radiographic features
⬜Imaging demonstrates enlargement of the muscle belly of one (or
more) occular muscles with involvement of the tendinous insertion.
Involvement of the tendinous insertion distinguishes it from thyroid
associated orbitopathy (TAO) in which the insertion point is spared.
Additional inflammation can be seen in surrounding tissues,
including the lacrimal gland. It can appear as infiltrative mass and
extends outside of the orbit via superior or inferior orbital fissures.
Extension into the cavernous sinus, meninges, and dura can occur.
MRI
⬜Reported signal characteristics include
⬜T1: affected region typically iso to hypo intense
⬜T2: affected region typically hypo intense due to fibrosis and with
more progression of fibrosis it becomes more hypointense
⬜T1 C + (Gd): diffuse enhancement
PSEUDO TUMOR
PSEUDO TUMOR
T1 T1 C + Fat sat
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