Neoplasms Flashcards

1
Q

Astrocytoma

A
  • glioma
  • pilocytic astrocytoma= WHO grade 1
  • diffuse astrocytoma= WHO grade 2
  • anaplastic astrocytoma= WHO grade 3
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2
Q

Oligodenroglioma

A
  • glioma
  • oligodendroglioma= WHO grade 2
  • age 42
  • cerebral white matter
  • fried egg appearance
  • presents with seizures
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3
Q

Ependymoma

A
  • glioma
  • most present during first two decades of life
  • spinal cord ependydmomas usually tumors of adults
  • true rosettes on histology
  • WHO grade 2
  • obstructive hydrocephalus
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4
Q

Medulloblastoma

A
  • glioma
  • grade 4
  • most common malignant brain tumor in children (3-8yo)
  • 50% survival rate
  • chromosome 17 deletions/mutations
  • Homer Wright rosettes
  • obstructive hydrocephalus
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5
Q

Meningioma

A
  • meningeal tumor
  • WHO grade 1
  • women in their 50s
  • may penetrate dura, occlude venous sinuses, invade bone and cause hyperostosis
  • push and distort underlying brain or cord
  • NF2 gene mutation, 22q loss
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6
Q

Shwannoma

A
  • slow growing
  • found on cranial nerve 8
  • also found on spinal nerve roots
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7
Q

Pilocytic Astrocytoma

A
  • most common CNS neoplasm of childhood
  • usual sites: cerebellum, optic pathway, hypothalamus, thalamus, spinal cord, temporal lobe
  • histopathology: elongated hairlike fibers, rosenthal fibers
  • genetics: BRAF:KIAA
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8
Q

Diffuse Astrocytoma

A
  • age 30-40
  • WHO grade 2
  • cerebral hemispheres, rarely post. fossa
  • ill-defined borders, not surgically resectable
  • genetics: IDHI mutation, 1p/19q, p53/ATRX
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9
Q

Anaplastic Astrocytoma

A
  • mean age 45 yrs
  • WHO grade 3
  • cerebral hemispheres in adults
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10
Q

Anaplastic Oligodendroglioma

A
  • anaplastic oligodendroglioma= WHO grade 3
  • mean onset 48
  • elevated MIB-1 rate
  • genetics: 1p19q codeletion
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11
Q

Glioblastoma (GBM)

A
  • 15% of all intracranial neoplasms
  • age 62 for primary GBM (progresses more quickly though)
  • age 45 for secondary GBM
  • WHO grade 4
  • cerebral hemispheres
  • follows white matter highways
  • primary genetics: EGFR8
  • secondary genetics: anaplastic astrocytoma with 10q loss
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12
Q

IDH1/2 Mutations

-prognosis

A
  • powerful prognostic factor
  • not present in non-neoplastic situations
  • IDH1 negative anaplastic astrocytomas do worse than IDH1 mutations
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13
Q

Papilledema

A
  • engorged retinal veins
  • due to inc ICP
  • LP could lead to herniation
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14
Q

Neoplasms of Childhood ______ metastasize to the brain.

A

-rarely

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