Mass Lesions Flashcards

1
Q

primary CNS tumors

A

common in childhood

high incidence 65-74

children: typically below tantrum (adults opposite)

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2
Q

why do symptoms develop from primary CNS tumors? (6)

A
  1. destruction
  2. space occupying (increased ICP)
  3. blocking flow (hydrocephalus)
  4. angiogenesis (disrupts BBB)
  5. decreased blood supply (compromised perfusion)
  6. herniation (increased ICP)
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3
Q

risk factors for primary CNS tumor

A

history of radiation to head

genetically inherited dz

HIV (CNS lymphoma is AIDS defining)

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4
Q

symptoms fo primary CNS tumor

A

slowly progressive (symptomatic late)

  1. HA (tension, worse @nite)
  2. personality/mood change, cognitive impairment
  3. decreased appetite or nausea
  4. seizures
  5. diplopia
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5
Q

signs of primary CNS tumor

A

cognitive dysfunciton

weakness

sensory loss

aphasia/apraxia

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6
Q

diagnostic SOC primary CNS tumor

A

MRI + contrast

can CT, PET, biopsy

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7
Q

types of primary tumors (9)

A
  1. glioblastoma multiforme
  2. astrocytoma
  3. meningioma
  4. CNS lymphoma
  5. acoustic neuroma
  6. oligodendrogliomas
  7. ependymomas
  8. pituitary adenomas
  9. primitive neuorectodermal tumors
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8
Q

glioblastoma multiforme

A

MC, most progressive

rapidly progressive, adults and cerebral hemispheres

arise de nova, develop from lower grade

fatal in 3 mo, optimal: CXT/XT 12mo

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9
Q

astrocytoma

A

agressive or indolently, but typically advanced grade

adults, cerebral invasion, symptoms by invasion/compression/destruction

sx,XT, CXT all considered

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10
Q

meningiomas

A

contiguous with meningitis, 90% benign

typically compress and irritate tissue = seizure

recur if not recited completely

XT or Sx only

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11
Q

CNS lymphoma

A

B cell NHL, solitery lesions

can be in immunocompetent or immunocompromised – esp. IVDA/HIV +

responsive to methotrexate and chemo/radiation

avoid steroids

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12
Q

acoustic neuroma

A

extra axial tumors of vestibular/choclear nerves

large before symptomatic

ipsilateral hearing loss, tinnitus, vertigo, HA, weakness

curable with excisions

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13
Q

oligodenrogliomas

A

young - middle age adults

good prognosis

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14
Q

ependymomas

A

intraventricular masses with extension in subarachnoid space

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15
Q

pituitary adenomas

A

chemically active or destruction

macro adenoma, micro adenoma

visual disturbance common (optic chasm)

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16
Q

primitive neuorextodermal tumors

A

posterior fossa

spreads widely

17
Q

surgical tx primary CNS tumor

A

done with intent to cure

no spread

18
Q

when is surgery CI

A

brainstem tumor
high risk of debilitating neuro dysfunction
lesions are muslticola

19
Q

gamma knife

A

radiosurgery

multiple radiation beams sent in and converge on one location

zaps tumor

20
Q

medical tx of primary CNS tumor

A

high dose steroids (decrease edema, decadron)

AED

radiation/chemo (CXT not used bc can’t cross BB)

21
Q

mc sources of CNS mets

A
lung
breast 
kidney 
melanoma 
GI
22
Q

why are mets more likely to have acute symptoms

A

more rapid growth
mor vasogenic edema
more likely to hemorrhage

23
Q

diagnosis of cns mets

A

MRI w/ and w.o contrast

24
Q

tx of CNS met

A

single: surgery + XT
multiple: discussion of prognosis

25
Q

primary CA metastasis to meninges and cord

A

leptomeningeal mass

26
Q

MC primaries of leptomeningeal mass

A

breast
lymphoma
leukemia

27
Q

symptoms leptomeningeal mass

A
ataxia/gait changes 
HA
disturbed sensorium
memory issues 
incontinence
28
Q

diagnostics of leptomeningeal mass

A

LP, CT, MRI

29
Q

tx leptomeningeal mass

A

poor prognosis

sz for planet of ommaya pump
XT, Cath CXT