Malignant tumor w/ notochordal differentiation
histology: physaliphorous cells (containing intracellular mucin)
high recurrence rate
CT - well-circumscribed; lytic, irregular intratumoral calcifications, ± enhancement
MRI - T1 - isointense; T2: hyperintense; T1C: hetero- enh. w/ honeycomb
radioresistant; Tx → Qx en bloc
dDx LGG/nml/reactive tissue is challenging
mts vs. glioma - 👍 on frozen
astro vs. ODG: artifact → miss Dx; “fried egg” (artifact of formalin fix) NOT present on frozen
glioma grading: sampling bias → undergrading; ± overgrading
radionecrosis vs. GBM: both my be present
lymphoma vs. SCLC: may resemble on frozen
Common first Sx
1st sz in pts >20 y/o → aggressively r/o SOL
if imaging ⊖ → should repeat later
congenital; arise from splitting of arachnoid membrane; ♂>♀
fluid is identical to CSF; not communicate w/ vent. or SS
two types: simple (meningothelial cells [arachnoid] → CSF secretion); complex (neuroglia, ependyma & other)
⊕ EMA, ⊖ CEA
Imaging: bone remodeling; CSF on CT/MRI; ± septations;
if incidental fi in adults → single f/u in 6–8 m (r/o ↑ size) if aSx
Tx: Qx if Sx
Type I: (MC)
Small, biconvex, in ant. temp. tip.
No mass effect.
Communicates w/ SS on cisternogram (WS-CTC)
± aSx; Tx: observation; Qx if Sx;
Type II:
prox. & intermed. seg. of Sylvian fissure.
open insula → rectangular shape
Partial communication on WS-CTC.
Type III:
entire Sylvian fissure.
MLS.
± bony expansion
minimal communication on WS-CTC.
Skin lesions
Tumors
Other features
Café au lait spots, freckles, neurofibromas
Optic gliomas, schwannomas, meningiomas
Learning disabilities, endocrine abnormalities, Dural ectasia
No skin lesions
Vestibular schwannomas, meningiomas, ependymomas
Hearing loss, mental retardation
10, 20, 30, Sick and Weary, 40, 50, Needing Help Quickly, 60, 70, Mostly Healthy, 80, 90, Perfectly Fine, 100, Divine.
ranges 0 - 5
0 - healthy; 5 is dead
dominant parietal lobe lesion
agraphia w/o alexia (can't write but can read)
left-right confusion
digit agnosia (can't identify finger by name
acalculia
Mnemonic: "A Lefty Digits Calculator"
Grading of meningioma invasion to SSS
Type I - attachment to lat. wall of sinus.
Type II - invasion of lat. recess.
Type III - invasion of lat. wall.
Type IV - invasion of lat. wall & roof.
Type V - total sinus occlusion, contral. wall spared.
Type VI - total sinus occlusion, invasion of all walls.
stacked arrangements of elongated palisading nuclei alternating w/ anuclear zones containing cell processes
These Verocay bodies are typically found in the more densely packed Antoni A regions, rather than in the loose or microcystic Antoni B areas.
Schwannomas
Pseudopalisading necrosis in a GBM characterized by a garlandlike arrangement of hypercellular tumor nuclei (arrows) lining up around irregular foci of tumor necrosis (n) containing pyknotic nuclei (arrowheads). Note tumor vessel (v).
GBM