Pathology of Brain Tumors Flashcards

1
Q

Two main age groups that get CNS tumors?

How do they differ in terms of location?

A

Kids: first two decades of life –> infratentorial

Older adults: 60s and 70s –> supratentorial

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2
Q

Features of grade II tumor?

A

Increased cellularity

Nuclear atypia

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3
Q

Features of grade III tumor?

A

Anaplastic tumor
Increase cellularity
Nuclear atypia
MITOSES

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4
Q

Histological features of glioblastoma multiforme (infiltrative/diffuse astrocytoma)?

A

Grade IV - all features of grade III + following:

Pseudopalisading necrosis - central necrosis with “stacked” cells on the edge

Vascular/endothelial proliferation

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5
Q

Gross and histological features of pilocytic astrocytoma (non-infiltrate/circumscribed astrocytoma)?

A

Cystic nodule with mural nodule.

Biphasic appearance with compact and loose “piloid” processes.

Rosenthal fibers - eosinophilic EXTRACELLULAR non-cytoplasmic inclusions.

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6
Q

Oligodendroglial tumors - what are the molecular markers necessary?

Prognosis relative to GBM?

Histological feature?

A

Deletion of chromosomes 1p/19q

Better prognosis–more chemosensitive!

Fried-egg appearance with ONLY oligodendrogliomas.

Oligoastrocytomas have BOTH fried eggs and astrocytoma components.

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7
Q

Where do ependymomas usually localize?

Prognosis?

A

To posterior possa, usually in children.

Prognosis based on:

  • Location: supratentorial worse location because blocks drainage
  • Age: young than 3 cannot undergo radiation
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8
Q

Histological features of ependymomas?

A

Perivascular pseudorosettes

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9
Q

Myxopapillary ependymoma

A

The ONLY GRACE I EPENDYMOMA.

Localizes UNIQUELY to conus/cauda equina/filum terminale

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10
Q

Etiology of medulloblastoma? Localization?

Clinical progression and histology?

A

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

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11
Q

Meningioma

Commonly affected population?
Histology?
Imaging?

A

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”

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12
Q

Craniopharyngioma

Commonly affected population?
Location?
Imaging?
Histology?

A

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)

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13
Q

Schwannoma

Location
Histological finding

A

Cerebellopontine angle –> bilateral acoustic schwannomas –> auditory symptoms

Verocay bodies - acellular area with palisading cells

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14
Q

NF2

Genetics
Associated tumors

A

Autosomal dominant, Merlin gene on chromosome 22

  • Bilateral acoustic schwannomas at cerebellopontine angle
  • Multiple meningiomas
  • Ependymomas (spinal)
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