Pathology of Brain Tumors Flashcards
Two main age groups that get CNS tumors?
How do they differ in terms of location?
Kids: first two decades of life –> infratentorial
Older adults: 60s and 70s –> supratentorial
Features of grade II tumor?
Increased cellularity
Nuclear atypia
Features of grade III tumor?
Anaplastic tumor
Increase cellularity
Nuclear atypia
MITOSES
Histological features of glioblastoma multiforme (infiltrative/diffuse astrocytoma)?
Grade IV - all features of grade III + following:
Pseudopalisading necrosis - central necrosis with “stacked” cells on the edge
Vascular/endothelial proliferation
Gross and histological features of pilocytic astrocytoma (non-infiltrate/circumscribed astrocytoma)?
Cystic nodule with mural nodule.
Biphasic appearance with compact and loose “piloid” processes.
Rosenthal fibers - eosinophilic EXTRACELLULAR non-cytoplasmic inclusions.
Oligodendroglial tumors - what are the molecular markers necessary?
Prognosis relative to GBM?
Histological feature?
Deletion of chromosomes 1p/19q
Better prognosis–more chemosensitive!
Fried-egg appearance with ONLY oligodendrogliomas.
Oligoastrocytomas have BOTH fried eggs and astrocytoma components.
Where do ependymomas usually localize?
Prognosis?
To posterior possa, usually in children.
Prognosis based on:
- Location: supratentorial worse location because blocks drainage
- Age: young than 3 cannot undergo radiation
Histological features of ependymomas?
Perivascular pseudorosettes
Myxopapillary ependymoma
The ONLY GRACE I EPENDYMOMA.
Localizes UNIQUELY to conus/cauda equina/filum terminale
Etiology of medulloblastoma? Localization?
Clinical progression and histology?
Neuroectoderm
Localized to cerebellum, usually vermis
Can enter 4th ventricle to cauda equina termed “drop metastasis”
Would see small round blue cells and homer wright reosettes
Meningioma
Commonly affected population?
Histology?
Imaging?
Older women - most common BENIGN CNS tumor in adults
If affect younger, often associated with NF2
Whorled cells that can calcify and turn int psammoma bodies
Imaging: bony hyperostosis that overlies dura with “dural tail”
Craniopharyngioma
Commonly affected population?
Location?
Imaging?
Histology?
Children/first two decades of life
Location: suprasellar region –> can compress optic chiasm to cause bilateral hemianopsia
Imaging: cystic component with calcifications/cholesterol crystals
Histology: cystic spaces, calcifications, “wet” keratin (keratin without nuclei)
Schwannoma
Location
Histological finding
Cerebellopontine angle –> bilateral acoustic schwannomas –> auditory symptoms
Verocay bodies - acellular area with palisading cells
NF2
Genetics
Associated tumors
Autosomal dominant, Merlin gene on chromosome 22
- Bilateral acoustic schwannomas at cerebellopontine angle
- Multiple meningiomas
- Ependymomas (spinal)