WT - Neuro Neoplasms Flashcards

1
Q

adult primary brain tumors

A
glioblastoma multiforme
oligodendroglioma
meningioma
hemangioblastoma
pituitary adenoma
schwannoma
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2
Q

childhood primary brain tumors

A
pilocytic astrocytoma 
medulloblastoma
ependymoma
craniopharyngioma
pinealoma
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3
Q

glioblastoma multiforme

A
  • most common ADULT
  • highly malignant
  • @ cerebral hemospheres
  • can cross corpus callosum (butterfly glioma)

histo:
- astrocyte origin (GFAP)
- pseudopalisading cells bordering central necrosis/hemorage/microvasc prolif

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4
Q

oligodenroglioma

A
  • ADULT
  • rare, slow growing
  • @frontal lobes
  • often calcified

histo:

  • oligodendrocyte origin
  • fried egg
  • chicken wire capillary
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5
Q

meningioma

A
  • ADULT
  • common, benign
  • F>M
  • @surfaces of brain and in parasagittal region
  • dural attachment (tail)

sx:

  • usu asymptomatic
  • seizures or focal neuro signs

histo:

  • arachnoid cell origin
  • spindle cells concentrically arranged in a whorled pattern
  • psammoma bodies

tx: reaction and/or radiosurgery

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6
Q

hemangioblastoma

A
  • ADULT
  • often cerebellar
  • VHL when found w/ retinal angiomas
  • EPO prod –> sec polycythemia

histo:
- blood vessel origin
- thin-walled capillaries
- minimal intervening parenchyma

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7
Q

pituitary adenoma

A
  • ADULT
  • nonfxn (mass effect –> bilateral hemianopia) or fxn (hormone prod)
  • pituitary apoplexy –> hypER or hypOpituitarism

histo: hyperplasia of only one type of endocrine cells in pituitary (commonly lactotrophs, less comm somatotropin (GH))
tx: DA agonist, transsphenoidal resection

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8
Q

Schwannoma

A
  • ADULT
  • @ cerebellopontine angle
  • benign
  • CN V, VII, VIII or any peripheral n.
  • often VIII in internal acoustic meatus (vestibular schwannoma)
  • bilateral vestibular schwannomas in NF-2

histo: Schwann cell origin (S-100), biphasic, dense, hypERcellular areas containing spindle cells, alt w/ hypOcellular. myxoid areas
tx: resection or stereotactic radiosurgery

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9
Q

pilocytic astrocytoma

A
  • most comm primary brain tumor in CHILD
  • low-grade astrocytoma
  • well-circumscribed
  • @posterior fossa (cerebellum
  • also may be supratentorial
  • benign, good prognosis

histo:
- astrocyte origin
- GFAP +
- rosenthal fibers (eos, corkscrew fibers, cystic + solid (gross)

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10
Q

medulloblastoma

A
  • most comm MALIGNANT brain tumor in CHILD
  • @ cerebellum

sx:

  • can compress 4th ventricle –> noncommunicating hydrocephalus –> HA –> papilledema
  • cerebellar vermis involvement –> truncal ATAXIA
  • “drop metastases” to spinal cord

histo:

  • form of primitive neuroextodermal tumor (PNET)
  • homer-wright ROSETTES
  • small blue cells
  • synaptophysin +
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11
Q

ependymoma

A
  • CHILD
  • @ 4th ventricle –> hydrocephalus
  • POOR prognosis

histo:

  • ependymal cell origin
  • perivascular pseudo rosettes
  • rod-shaped blepharoplasty (basal ciliary bodies) near nucleus
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12
Q

craniopharyngioma

A
  • CHILD
  • most comm childhood SUPRATENTORIAL tumor
  • may be confused w/ pituitary adenoma (both–>bitemporal hemianopia)

histo:

  • derived from remnants of Rathke pouch (ectoderm)
  • calcification=common
  • CHL crystals in “motor oil” like fluid within tumor
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13
Q

pinealoma

A
  • CHILD
  • tumor of pineal gland

sx:

  • PARINAUD syndrome (compression of tectum –> vertical gaze palsy)
  • obstructive hydrocephalus (compression of cerebral aqueduct)
  • precocious puberty in males (hCG prod)

histo:
-sim to germ cell tumors (testicular seminoma)

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