Brain Tumors Flashcards

1
Q

Most CNS tumors originate where?

A

**metastatic from another site **

bladder, lung, breast, kidney, liver, and melanoma

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2
Q

Most common primary brain tumors? (2)

A

Giloblastoma multiforme (GBM)

menigioma

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3
Q

How do you distinguish a primary brain tumor from a metastasis to the brain?

A

PBT:

  • Poorly circumscribed
  • Usually single
  • Location varies by specific type

Metastasis:

  • generally well circumscribed
  • often multiple
  • Usually located in the junction between gray and white matter
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4
Q

Most common CNS tumors in children? (2)

A
  • Medulloblastoma
  • Astrocytoma

CNS tumors are 2nd most common neoplasm in children

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5
Q

Any treatment that follows the primary treatment is called what?

A

adjuvant treatment

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6
Q

WHO Grade I

A

generally low proliferative potential– possible to cure following resection alone

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7
Q

WHO Grade II

A

generally infiltrative but low proliferative activity

(cells are starting to move into places that they shouldn’t be)

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8
Q

WHO Grade III

A

general histological evidence of malignancy (nuclear atypia and much mitotic activity)

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9
Q

WHO Grade IV

A

cytologically malignant, mitotically active, necrosis prone. Rapid pre and post operative disease progression

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10
Q

pilocytic astrocytoma

A

Grade I

Low proliferative potential

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11
Q

A child patient presents with a primary brain tumor that is in the posterior fossa (common to cerebellum), and you hear from the oncologist that the patient has a good prognosis. What do they likely have? WHO Grade?

A

pilocyclic astrocytoma

(Grade I)

Morphologic features:–often cystic–bipolar cells with long hair-like processes–rosenthal fibers–biphasic: loose areas and dense areas

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12
Q

Rosenthal fibers are associated with what what type of primary brain tumor? What color do they appear on H and E?

A

pilocytic astrocytoma

rosenthal fibers are eosinophilic (red) and composed of several proteins including GFAP

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13
Q

diffuse astrocytoma

A

Low proliferative potential but infiltrative

Grade II

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14
Q

anaplastic astrocytoma

A

shows more cellular regions–more pleomorphism, more mitoses

Grade III

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15
Q

GFAP

A

glial fibrillary acidic protein

Principle intermediate filament in mature astrocytes

If elevated, indicates damage to astrocytes

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16
Q

Difference between primary GBM and secondary GBM

A

secondary GBM begins as a anaplastic astrocytoma

primary GBM is direct diagnosis

17
Q

pseudopalisading necrosis

A

a key feature of a primary GBM

18
Q

glioblastoma

A

Grade IV

  • variation in appearance in different areas
  • necrosis
  • vascular proliferation
19
Q

A patient presents with seizures and an MRI indicates a sharply circumscribed hemispheric masses, and biopsy reveals a highly vascularized tumor, round nuclei with cytoplasmic halos and some calcification. What type of neoplasm?

A

Oligodendroglioma

20
Q

Medulloblastoma

A

WHO grade IV

Clinical features: Usually in children, usually in cerebellum–Very radiosensitive!– isochromosome (17)(q10) = poor prognosis

Morphologic features: Well-circumscribed Histologic features: Small, dark, elongated, anaplastic cells–Homer-Wright rosettes

21
Q

A child patient presents with headach, and morning vomitting that gets worse with time. In addition, the patient is having trouble with motion sickness and back pain. What should you be worried about?

A

Medulloblastoma

(Remember to look for isochromosome 17 i17, which if present is a poor prognosis)

22
Q

Meningioma

A

Second most common primary brain tumor

Clinical features:–benign tumor of arachnoid cells–slow-growing, benign–cured by resection

Morphologic features:–attached to dura, compresses brain–syncytial pattern–psammoma bodies

23
Q

syncytial pattern

A

sworreling

24
Q

psammoma bodies

A

calcium deposits