Neuropath of Tumors I Flashcards

1
Q

Name these Diffuse Astrocytomas

Grade II

Grade III

Grade IV

A

Diffuse Astrocytomas

Anaplastic Astrocytomas

Glioblastomas

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2
Q

Grade II Astrocytomas Age of Onset Survival ___ Atypia ___ Mitosis Path shows _____

A

30 80 Months Yes Atypia, No Mitoses Angulations

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3
Q

Grade III Anaplastic Astrocytomas Age of Onset Survival ___ Atypia ___ Mitosis

A

40 30 Months Yes Atypia, Yes Mitoses

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4
Q

Grade IV Glioblastomas Age of Onset Survival ___ Atypia ___ Mitosis Path shows focal areas of ____ and ______ ____ which are infiltrating microvessels

A

40-55 14 Yes Atypia, Yes Mitoses necrosis; glomerular tufts

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5
Q

Primary GBM tumors overexpress ____ in 60% of cases

A

EGFR

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6
Q

Secondary GMB tumors (transformed from grades II/III) overexpress ___ and ___

A

p53; IDH1/2

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7
Q

GBM tumors which overexpress ___ have a better prognosis

A

IDH1

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8
Q

Diffuse Astrocytomas are not _____ therefore making them difficult to resect

A

Encapsulated

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9
Q

Pliocytic Astrocytomas are separate from Diffuse Astrocytomas for three reasons 1) They ____ invade surrounding tissue 2) They ____ progress to anaplastic Grade III 3) Have a _____ prognosis

A

1) Don’t 2) Don’t 3) Better

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10
Q

Genetics of Pliocytic Astrocytomas Gain on ____ which results in the tandem duplication of _____ and ______, producing a novel oncogene activating MAPK

A

7q34; BRAF; KIAA1549

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11
Q

Pliocytic Astrocytoma Pathology Have a ____ architecture with a _____ and a ____ area.

A

biphasic; compact; spongy

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12
Q

____ areas of the biphasic architecture of Pliocytic Astrocytoma show ______ granules (stain) _____ fibers may be present

A

Spongy; eosinophilic Rosenthal

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13
Q

Oligodendrogliomas present in a _____ cellular pattern

A

diffuse

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14
Q

Oligodendrogliomas all begin at Grade __ or higher

A

II

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15
Q

Oligodendroglioma Path- show clear cytoplasm around the nucleus in a _____ ____ pattern (this is seen in normal oligodendrocytes but in much lower cellularity). The thin vessels supplying the tumor are called _____ ____

A

fried egg; chicken wire

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16
Q

Oligodendroglioma genetics- LOH on chromosomes ___ and ___. This change indicates a _____ prognosis

A

1p; 19q favorable

17
Q

Ependymomas occur most commonly in ______ (demographic)

A

children and young adults

18
Q

Ependymomas occur most commonly in the ______ and the ____ ____ (location

A

4th ventricle; spinal cord

19
Q

Ependymoma path- Frequently, ________ are present with cells lining a ____. Rarely are true _____ seen around a ____.

A

pseudorosettes; vessel rosettes; hole

20
Q

All embroyonal tumors are Grade __

A

IV

21
Q

Medulloblastomas occur in _____ (demographic) in the _____ (location)

A

children, vermis of cerebellum

22
Q

Medulloblastomas can form discrete masses in the _ ______

A

4th ventricle

23
Q

Medulloblastomas arise from granular precursor cells in the ____ ____ _____

A

external granular layer

24
Q

This type of rosettes are found in Medulloblastomas and are a sign of ____

A

Homer Wright; neuronal differentiation

25
Q

_____ increases your risk of Schwannoma and patients often present with _____/____ Schwannoma

A

NF2; acoustic/vestibular

26
Q

Multiple neurofibromas are associated with ____

A

NF1

27
Q

50% of patients with NF2 will have

A

meningiomas

28
Q

Meningiomas arise from which cell type

A

arachnoid cells

29
Q

Meningioma path- Present in cellular shapes called _____; calcified _____ are called _____ _____

A

whorls; psammoma bodies

30
Q

The large majority of Meningiomas, Schwannomas, and Neurofibromas are Grade

A

I

31
Q

What are the two types of Neurofibromas? (where disease manifests)

A

Dermal and interneural

32
Q

Schwannomas _____ nerves while Neurofibromas _____ axons

A

displace; incorporate