SECRETS Neurology - Brain Tumors & Neurocutaneous Disorders Flashcards

1
Q

brain tumor sx

A

mass effect - tumor compressing brain

hydrocephalus, papilledema, nausea/vomiting, headache, mental status changes

seizures, focal neuro signs, dementia

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2
Q

most common location of tumor in adults? kids?

A
adult = supratentorial
kids = infratentorial
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3
Q

most common primary tumor in adults? kids?

A
adults = astrocytoma
kids = astrocytoma

metastases > primary

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4
Q

astrocytoma type with worst prognosis

A

glioblastoma multiforme

other lower grades of astrocytoma (juvenile pilocytic astrocytoma, anaplastic astrocytoma) may evolve into glioblastoma multiforme

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5
Q

glioblastoma multiforme histology

A

psueodpalisading arrangement of tumor cells

crosses over into both hemispheres

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6
Q

calcifications on intracranial mass?

A

meningioma

oligodendroglioma

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7
Q

meningioma

A

calcifications
frontal lobe

whorled pattern with psammoma bodies

benign tumor of arachnoid cells of meninges
external to brain, can be resected easily

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8
Q

oligodendroglioma

A

calcifications
frontal lobe

fried egg appearance

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9
Q

second most common primary tumor in adults? kids?

A
adults = meningioma
kids = medulloblastoma
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10
Q

medulloblastoma

A

malignant tumor of cerebellum

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11
Q

lomustine, carmustine

A

alkylating agents = nitrosoureas

cross BBB

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12
Q

what can cross BBB

A

small
lipid soluble
nonpolar

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13
Q

tuberous sclerosis

A

rare AD neurocutaneous disorder

epileptogenic subependymal tumors

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14
Q

tuberous sclerosis sx

A

seizures, mental retardation
ash-leaf spots = multiple, ovate, hypopigmented macules
shagreen patches = rough skin patch

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15
Q

tuberous sclerosis tumor assoc

A

renal angiomyolipoma
cardiac rhabdomyoma (hx cardiac murmur at birth)
CNS hamartomas
subependymal giant cell astrocytomas

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16
Q

neurofibromatosis I

A

cafe au lait spots
lische nodules
multiple neurofibromas

AD mutation on chr 17

17
Q

neurofibromatosis II

A

tinnitus & sensorineural deafness due to bilateral schwannomas (impinge CNVIII)

mutation on chr 22