Tumors Flashcards

1
Q

fibrillary astrocytoma

A
  • found in cerebral hemispheres; cortex w/ no specificity for any particular region
  • young adults 20-40yo
  • present w/ seizures, headache; no focal neuro deficits
  • imaging = diffuse tumor; poor prognosis
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2
Q

glioblastoma multiforme

A
  • poor prognosis = 8-10m to live
  • older adults
  • arises w/o pre-existing tumor; rapid progression
  • hallmark = necrosis; pronounced mass effect and edema
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3
Q

pilocytic astrocytoma

A
  • young adults and kids
  • in the cerebellum; could get into optic pathway
  • presents w/ gait problems; hydrocephalus if big enough to obstruct CSF flow
  • appears as solid, brightly contrasted mass w/ associated cyst
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4
Q

brainstem glioma

A
  • seen up to about age 20; most common pediatric glioma
  • in pons, medulla
  • sensory problems, cardio/resp problems
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5
Q

oligodendroglioma

A
  • young and middle-aged adults
  • lesion in cerebral hemisphere = where white matter is = where myelin is
  • generally w/in frontal and temporal lobes
  • commonly see calcification w/in tumor
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6
Q

ependymoma

A
  • ependymal cells line the ventricular system and spinal cord
  • if tumor in ventricles = kid pt
  • tumor in spinal cord = adult pt
  • if at filum terminale = myxopapillary ependymoma
  • will see rosettes in microscopy
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7
Q

colloid cyst

A
  • 3rd ventricle; benign
  • seen in adults 20-50yo
  • causes non-communicating hydrocephalus = lateral ventricles dilated
  • present w/ headaches; possibly positional
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8
Q

central neurocytoma

A
  • intraventricular - usually attached to septum pellucidum
  • adults age 25-30
  • N/V, headache from obstructive hydrocephalus
  • slow-growing, benign
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9
Q

medulloblastoma

A
  • in kids up to about age 20
  • cerebellum
  • malignant but very radiosensitive
  • good prognosis if dx early and do radiation therapy
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10
Q

primary CNS lymphomas

A
  • seen in immunosuppressed pts = HIV, SLE highest risk
  • after age 60 usually
  • key feature = invading other regions of the brain i.e. crossing the corpus callosum
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11
Q

craniopharyngioma

A
  • seen in young kids (10-14) and elderly (60+)
  • located above sella tursica = where optic chiasm is = present w/ bitemporal hemianopsia i.e. tunnel vision
  • benign (not a glial cell); can cause non-communicating hydrocephalus
  • commonly calcify
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12
Q

most common tumors in kids?

A
  • medulloblastomas
  • fibrocytic astrocytomas
  • craniopharyngiomas
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13
Q

meningioma

A
  • benign, seen in adults (more women b/c tumor has estrogen receptors)
  • usually attached to dura
  • can be in any region
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14
Q

metastatic brain tumors

A
  • lung, breast, skin most common; also kidney and GI
  • show up as multiple lesions on imaging; a primary malignancy shows only one lesion
  • frequent site = meninges
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15
Q

schwannomas

A
  • benign; from neural crest cells
  • SOL in brainstem, spinal cord
  • CNVIII involvement = hearing losses, tinnitus = acoustic neuroma
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16
Q

von Hippel Lindau disease

A
  • autosomal dominant disease
  • hemangioblastomas in cerebellum and retina
  • tumors secrete erythropoietin so RBCs will be elevated
  • disease is benign but increased risk of renal carcinoma and pheochromocytoma
17
Q

tuberous sclerosis

A
  • autosomal dominant disease
  • form cortical tubers and SEGA tumors in cortex –> start at brain covering and protrude inward
  • generally see epilepsy/seizures
  • 3 types of tumor associated:
    1. cortical tubers; 2. subependymal nodules; 3. giant cell astrocytomas
18
Q

neurofibromatosis type 1

A
  • type 1 = lacking NF1 gene
  • autosomal dominant disorder
  • plexiform and solitary neurofibromas; gliomas of optic n.
  • Lisch nodules in iris
  • café au lait spots
19
Q

neurofibromatosis type 2

A
  • autosomal dominant disorder
  • CNVIII schwannomas (acoustic neuromas), multiple meningiomas and ependymomas of spinal cord common
  • hearing loss, facial m. weakness, dizziness, poor balance, cataracts at early age