Extra axial lesions
Meningioma
Hemangiopericytoma
Meningial metastasis
Schwannoma
Arachnoid cyst
Dermoid cyst
Epidermoid cyst
Signs of extra axial
location
CSF cleft
Gray white matter buckling
Broad dural base(dural tail)
Displaced subaracnoid vessels
Displace and expand subaracnoid space
Bony reaction
Broad dural base
Grey white matter
buckling
CSF cleft
• There is a CSF cleft (yellow arrow).
• The subarachnoid vessels that run on the surface of the
brain are displaced by the lesion (blue arrow).
• There is gray matter between the lesion and the white
matter (curved red arrow).
• The subarachnoid space is widened because growth of
an extra-axial lesion tends to push away the brain
broad dural base or a dural tail of enhancement as is
typically seen in meningiomas.
There is hyperostosis in the adjacent bone and the
lesion enhances homogeneously
MENINGIOMA
Location
Supratentorial (90%):
Para sagittal/convexity (45%),
sphenoid ridge (15-20%),
olfactory groove (5-10%),
parasellar (5-10%)
Infratentorial (8-10%): CPA most common
inside the dura:
Intraventricular, optic nerve sheath, pineal region
outside the dura: Paranasal sinus (most
common), nasal cavity, parotid, skin, calvarium
Convexity Parafalcine
Sphenoid Ridge Olfactory Groove and sella
Posterior Fossa Cerebellopontine angle
Morphology
Extra-axial mass with broad-based dural
attachment
Two basic morphologies
Globose = globular, well-demarcated
neoplasm with wide dural attachment
En plaque = sheet-like extension covering
dura without parenchymal invagination
En plaque
WHO grading
Common meningioma = WHO grade 1
very slow-growing tumors account for
75%
Atypical meningioma = WHO grade 2
Usually slow-growing but can recur.
Malignant meningioma = WHO grade 3
More malignant, faster-growing.
Radiographic Findings
Radiography:
Hyperostosis,
irregular cortex,
tumoral calcifications,
increased vascular
markings
CT Findings
NECT
Hyperostosis, irregular cortex,
tumoral calcifications,
increased vascular markings
Sharply circumscribed smooth mass
abutting dura
Hyperdense (70-75%), iso- (25%),
hypo- (1-5%)
Calcified (20-25%): Diffuse, focal,
sandlike, sunburst, globular, rim
Necrosis, cysts, hemorrhage (8-23%)
Rare lipoblastic subtype ~ negative
Hounsfield
Brain cysts & trapped pools of CSF
common
Peritumoral hypodense vasogenic
edema (60%)
CECT: > 90% enhance
homogeneously & intensely
MR Findings
TlWI
o Usually iso- to slightly hypointense with cortex
o Necrosis, cysts, hemorrhage (8-23%)
o Best to visualize gray matter "buckling“
T2WI
o Variable; sunburst pattern may be evident
o Best to visualize trapped hyperintense CSF
clefts (80%) &
Axial T1 C+ MR
vascular flow voids (80%) Axial Tl C+ MR shows
demonstrates
• FLAIR: Hyperintense peritumoral edema, heterogeneous
dural "tail" dural-based
enhancing
• T2* GRE: Best sensitivity for calcification mostly
• DWI: DWI, ADC maps ,variable in appearancehomogeneousl mass of
• Tl C+ cerebellopontine
y enhancing
o > 95% enhance homogeneously & intensely angle extending into
mass with
o Dural "tail" (35-80% of cases ): Non-specific the
o En plaque: Sessile thickened enhancing dura cortical
internal auditory
buckling.
canal but
Note dural
without obvious
"tail" (arrow).
widening.
Angiographic Findings
"Sunburst or radial"
appearance with
prolonged vascular
"stain"
DSA: "Mother-in-law"
sign ~ comes early, stays
late
Dural vessels supply
lesion core
Pial vessels (ACA, MCA,
PCA) may supply
periphery when
parasitized
Venous phase vital to
evaluate sinus
involvement
ATYPICAL AND MALIGNANT
MENINGIOMA
Dural based lesion locally invasive with areas of
necrosis & marked brain edema.
CT Findings
NECT
Hyperdense with minimal or no calcification
Marked perifocal edema & bone destruction
CT "Triad" of Malignant meningima
Extracranial mass, osteolysis, & intracranial .
tumor
CECT
Enhancing tumor mass
Prominent pannus or tumor, extending away from
mass termed "mushrooming"
MR Findings
TlWI
Indistinct tumor margins
Extending tumor
interdigitating with brain
FLAIR :
Marked peritumoral edema
DWI
Markedly hyperintense on DWI
Marked decrease in ADC
Correlates with histopathology
T1 C+ Sagittal T1 C+ MR
Axial
Enhancing tumor mass shows enhancing
FLAIRMR
Plaque like & may extend into tumor
demonstrates
brain, skull, scalp involving the scalp,
hyperintense
skull, &
tumor
underlying brain.
"mushrooming"
with hypointense
inwards
Brain edema
deforming
HEMANGIOPERICYTOMA
"angioblastic Location
Supratentorial: Occipital
meningioma,“ region most common
Lobular
Typically involve falx,
enhancing extra- tentorium, or dural sinuses
axial mass with
Rarely from skull base,
dural attachment, cranial nerve,
+/- skull erosion intraventricular
involvement
May mimic
meningioma, Dural "tail" commonly
seen, approximately 50%
but without Ca+
+ or hyperostosis
CT Findings
NECT:
Hyperdense extra-axial mass
with surrounding edema
Low density cystic or
necrotic areas are common
Calvarial erosion may be Axial CECT shows an
seen aggressive
appearing, lobular
No Ca++ or hyperostosis extra-axial mass with bone
erosion
CECT: (arrow), central
Strong, heterogeneous necrosis, and surrounding
edema,
enhancement typical of
hemangiopericytoma
MR Findings
TlWI
Heterogeneous mass,
isointense to gray matter
Flow voids may be seen
T2WI
Heterogeneous isointense
mass
Prominent flow voids are
common
Surrounding edema, mass
effect typical Axial T1 C+ MR shows
Hydrocephalus may be seen an avidly enhancing
Tl C+
mass
Marked enhancement, often
With areas of low
signal
heterogeneous
Dural "tail" may seen
intensity representing
necrosis
And extension through
the
Schwannoma
Benign encapsulated Location
nerve sheath tumor
composed of
All cranial nerves (exceptions:
differentiated neoplastic Olfactory, optic
schwann cells nerves) have myelinated
Cranial nerve schwann cell sheaths are
schwannoma: Slow- sites for intracranial
growing schwannomas
extra-axial mass
98% arise from cranial nerves
Displaces ("buckles") (predominately sensory)
cortex 90% arise from CN 8 (vestibular
CSF-vascular "cleft" portion)
10% other (5% CN 5; 7; motor
between tumor, brain nerve
Cyst with nodule schwannomas rare in absence
of NF2)
1-2% intracerebral
CT Findings
NECT
Noncalcified extra-axial mass
Iso/slightly hyperdense compared to brain
May enlarge bony foramina (lAC, foramen
ovale, facial nerve canal)
Parenchymal:
Well-delineated hypodense cyst +
isodense nodule,
variable Ca++
CECT: Strong, uniform enhancement
MR Findings
TlWI
Usually iso-, sometimes
mixed iso/hypointense
Less common: Intra tumoral
cyst (occasionally have fluid-
fluid level), hemorrhage
Marginal arachnoid cyst
T2WI
Hyperintense (nodule may
be isointense) Axial T2WI MR in a
Surrounding edema Axial T1 C+ MR with fat
patient with
common suppression shows the
Tl C+
diplopia shows
orbital apex mass
Enhances strongly a lobulated, well-
enhances
Cranial nerve schwannoma: delineated
strongly but
2/3 solid; 1/3 ring or mass at the orbital
inhomogeneous heterogeneously.
apex that
Parenchymal schwannoma: Schwannoma of
Nodule enhances strongly
expands superior
abducens
Identify even small sized orbital
nerve was found at
lesion fissure (curved
surgery
arrow),
extends posteriorly
Meningeal metastases
Meningeal metastases may involve the
pachymeninges (dura mater),
leptomeninges (arachnoid and pia mater)
or both.
Carcinomatosis of the dura mater,
common in carcinoma of the breast,lung,
melanoma
CT Findings
NECT
Any: May find hemorrhagic
hyperdensity
Sub-galeal space: Relative dense lesion
CECT
Skull M: Enhancing mass centered in
bone with osseous destruction, lacking
'benign" sclerotic border
Most are lytic; a few sclerotic (e.g., Axial CECT shows
prostate) diffuse, bilateral,
DM & LM: Both may appear as leptomeningeal
enhancing biconvex metastases.
masses displacing brain Morphology is
DM characterized by calvarial smooth rather
involvement than nodular
Carcinomatosis: CT is insensitive,
however
hydrocephalus may be early sign
MR
Findings
TlWI
SM: Hypointense marrow
lesion
DM & LM: Most masses
hypointense to gray matter
Sub-galeal space: Relative
hypointense lesion
T2WI Axial Axial TIC+ MR:
SM: Hyperintense marrow Tl C+ MR: Carcinomatosis
lesion; dura usually intact Enhancing skull w/tumor along
DM between skull &
metastasis folial pia
elevated hypointense dura
DM & LM: Most
involves both (white arrow) &
hyperintense relative to underlying dura also
gray matter and subarachnoid/
FLAIR overlying scalp. CSF coating
Diffuse hyperintense to
Superior ventricle (black
CSF
sagittal sinus is arrow),
occluded by cranial nerves
invasion (arrow). (open black
Fat-saturation arrows), brain
ARACHNOID CYST
Intra-arachnoid CSF-filled sac that does not
communicate with ventricular system
Sharply demarcated round/ovoid extra-axial
cyst that follows
CSF attenuation/signal
Location
50-60% middle cranial fossa (MCF)
10% cerebellopontine angle (CPA)
10% suprasellar arachnoid cyst (SSAC),
variable types
10% miscellaneous
(convexity,quadrigeminal)
CT Findings
NECT
Usually CSF density
Hyperdense if
intracyst hemorrhage
present
May expand,
thin/remodel bone
CECT: Doesn't
enhance
CTA: Posterior
displacement of MCA
in middle cranial
fossa
CT: Cisternography
may demonstrate
communication with
subarachnoid space
MR Findings
TlWI
Sharply-marginated extra-
axial fluid collection
isointense with CSF
"Mickey mouse ears"
appearance on coronal scans =
SSAC plus lateral ventricles
T2WI: Isointense with CSF
PD Isointense with CSF
FLAIR: Suppresses completely
with FLAIR
T2* GRE: No blooming unless Axial FLAIR MR shows Axial
hemorrhage present (rare) an extra-axial DWl MR
DWI: No restriction
cystic-appearing mass in shows no
T1 C+: Doesn't enhance
MRA: Cortical vessels
the restriction.
displaced away from calvarium middle cranial fossa Presumptive
MRV: Can demonstrate (arrows). diagnosis is
anomalies of venous drainage The temporal lobe arachnoid cyst.
is hypoplastic with Epidermoid
posteriorly displaced cyst would not
temporal horn. suppress
DERMOID CYST
congenital inclusion cysts
Location
Most often in sellar/parasellar/frontonasal
region
Posterior fossai midline vermis & 4th
ventricle
Intraventricular within tela choroidea in
lateral, 3rd, or 4th ventricles
Extracranial sites = spine, orbit
Ruptured: Subarachnoid/intraventricular
spread of contents
CT Findings
NECT
Round/lobulated, well-
delineated, cystic mass
Fat hypodensity
20% capsular Ca++
With rupture, droplets of
fat disseminate in cisterns,
may cause fat-fluid level Axial NECT shows
within ventricles hypodense, fat-containing
Skull/scalp dermoid
pineal region dermoid
expands diploe (black arrow) which has
Frontonasal: Bifid crista ruptured.
galli, large foramen cecum Fat droplets are present
+ sinus tract throughout subarachnoid
CECT: Generally no space (white arrows
enhancement
MR Findings
TlWI
Unruptured: Hyperintense on Tl WI
Ruptured: Droplets very hyperintense
on Tl WI
Fat suppression sequence confirms
Fat-fluid level in cyst, ventricles
common
Rare "dense" dermoid: Very
hyperintense on Tl WI
T2WI Axial T1WI MR of Axial T2WI MR
Unruptured: Heterogeneous, from ruptured dermoid ruptured dermoid
hypo- to hyperintense on T2WI
Ruptured: Typically hyperintense (black arrow). Fat (black
droplets on T2WI droplets are arrow) contents
Rare "dense" dermoid: Very present dispersed in
hypointense on T2
With hair: Fine curvilinear hypointense throughout subarachnoid space
elements subarachnoid W ventricular fat-
Tl C+: With rupture: Extensive MR
enhancement possible from chemical
space (white fluid levels,
meningitis arrows) with associated with
ventricular fat- chemical shift
fluid levels artifact
EPIDERMOID CYST
CSF-like mass insinuates cisterns,
encases nerves/vessels
Lobulated, irregular, "cauliflower-like"
mass with "fronds
Location
90% intradural, primarily in basal cisterns
Cerebellopontine angle (CPA) = 40-50%
Fourth ventricle = 17%
Para sellar/middle cranial fossa = 10-15%
Rarely in cerebral hemispheres = 1.5
CT Findings
NECT
Round/lobulated mass
> 95% hypodense, resembling
CSF
10-25% Ca++
Intradiplioc epidermoid: Bony
erosion with sharply
corticated margins
Rare variant = "dense"
epidermoid ,Secondary to Axial CECT shows non-
hemorrhage, high protein,
saponification of cyst debris to
enhancing, off-midline,
calcium soaps or iron- CSF isodense
containing pigment
CECT: Usually none although epidermoid within
margin of cyst may
show minimal enhancement
quadrigeminal cistern
MRI
TlWI
Often (75%) slightly
hyperintense to CSF
Lobulated periphery may be
slightly hyperintense
than the center
Uncommonly
Sagittal T1 WI MR
hyperintense to brain ("white
epidermoid") due to high demonstrates CSF
triglycerides & unsaturated
fatty acids isointense
hypointense to CSF ("black
epidermoid
epidermoid") due to Presence
of solid crystal cholesterol & expanding the fourth
keratin Lack of triglycerides
& unsaturated fatty acids ventricle.
T2WI:
Often iso
(65%) to
slightly
hyperintense
(35%) to CSF
Very rarely
hypointense
Axial T2WI MR Axial T2WI MR
due to
calcification, shows nearly CSF shows
viscous isointense nearly CSF
secretions, epidermoid isointense
iron pigments
expanding the epidermoid within
fourth ventricle. left
Axial DWl MR shows restricted
diffusion within left anterior
middle cranial fossa epidermoid.
Tl C+
Usually none although margin of cyst may
show
Minimal enhancement (35%)
With malignant degeneration changes into
enhancing tumor
Epidermoid Dermoid
content Squamousepithelial cells, Hair,fat,sweat glands
keratin,choelesterol
location Off midline Mid line
CPA most common Spinal canal most common
Parasellar,middle fossa Parasellar ,post fossa
Rupture Rare common
Age Mean 40 years Younger adults
CT density CSF density May have fat
Ca++ Uncommon common
Enhancement Occasionaly periphrally none
MRI CSF like signals Proteinaceous fluid
other 5-10 times more
commoner than dermoid
Cerebello Pontine Angle
tumor
meningioma schwannoma epidermoid
Epicenter Dural based IAC CPA
CT Hyper/iso dense iso hypo
Ca++ frequent none occasional
Int.aco.canal normal widended normal
T2w relative to 50%isodense hyper hyper
Gr M
Enhancement dense dense none
Reference
DI Brain
Neuro imaging osborn
Grainger
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