neuro-CNS tumors Flashcards

1
Q

most common CNS malignancies…

A
1. “Metastases are the most common CNS malignancy” – 
(lung most common, breast, kidney, GI)
2. Of intrinsic, gliomas most common
Others:
CNS lymphoma, meningiomas, 
Infectious (e.g. in AIDS patients)
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2
Q

how do CNS tumors present?

A

All due to mass effect on specific areas of brain, or increasing intracranial pressure

  • Progressive headache/ nausea
  • Cranial nerve involvement
  • Seizures, sensorimotor changes
  • Cognitive impairment
  • Visual field changes
  • Brainstem or uncal herniation leading to sudden death
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3
Q

what is an uncal herniation?

A

cerebellar tentorium (white area above cerebellum- seperates cerebral cortex from cerebellum) - uncal- pushes past this tenorium - can cause death

from temporal lobe herniating down into the brain stem

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4
Q

hemispheric and central diencephalic tumors cause…

A

Hemispheric and central diencephalic tumors – focal motor deficits occur in ~40%

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5
Q

hypothalamic tumors cause…

A

Hypothalamic tumors – neuroendocrine abnormalities, may impinge on the optic chiasm –>visual deficits

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6
Q

astrocytoma in the cerebellum, brain stem, visual pathway cause…

A

Astrocytomas of the cerebellum – weakness, tremor, ataxia
Astrocytomas of the brain stem – isolated cranial nerve deficits and contralateral hemiparesis
Astrocytomas of the visual pathways – strabismus, proptosis, nystagmus, or developmental delay

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7
Q

astrocytoma in the spinal cord causes…

A

Astrocytomas of the spinal cord – pain localized to the vertebral segments adjacent to the tumor, weakness, gait disturbance, and sphincter dysfunction; paresthesias and loss of sensation occur later in the disease course

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8
Q

intramedullary vs extramedullary spinal cord tumors

A

Intramedullary ~10%- arise from inside the spinal cord:
-Ependymoma most common intramedullary tumor; the remainder are other types of glioma

Extramedullary may be extradural or intradural
neurofibromas and meningiomas are relatively common, are benign, and may be intradural or extradural
…others are usually extradural

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9
Q

___ of pts with a brain tumor complain of what first?

A

1/3, HA … a progressive headache disorder or the new onset of headaches in middle or later life merits investigation if no cause is apparent

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10
Q

Dx of CNS tumor

A
  • MRI (bony artifacts complicate CT)
  • angiography: for solid mass vs aneurysm
  • brain biopsy
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11
Q

txt of brain tumor

A

Oncology, neurosurgery consults

Surgery, irradiation, chemotherapy, depending on tumor type

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12
Q

primary intracranial tumors

A

Most common/malignant
Glioblastoma multiforme (GBM) is the most common and most aggressive of the primary brain tumors
-in kids: medulloblastoma & brainstem glioma
-ependymoma

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13
Q

pseudotumor cerebri - what is it? symptoms? who does it effect?

A

“Idiopathic Intracranial Hypertension” (better term for this) -mild HAs
-Increase in CSF production/decrease in absorption= increased pressure
-optic nerve atrophy and visual loss (papilledema)
Mostly affects obese women of childbearing age (20x more common)

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14
Q

pseudotumor cerebri signs? early vs later

A

Early:
Headache, diplopia, visual complaints

Later:
Limited abduction from increased ICP
Visual loss, starting in inferior nasal visual fields

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15
Q

txt pseudotumor cerebri?

A

lower ICP and CSF volume, treat papilledema

  • Acetazolamide decreases CSF production
  • Steroids
  • Weight loss
  • Serial LPs to remove CSF pressure
  • **Peritoneal shunts, optic nerve sheath fenestration to relieve pressure
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16
Q

neurofibromatosis.. what is it? symptoms?

A

A.K.A. Von Recklinghausen Disease
neural tissue tumor
-genetic, arises spontaneousl. doesn’t mean you got from your parents but if you have it you will pass it on.
-Abnormal NF1 gene on Chr. 17, with decreased tumor suppression activity
-NF2 gene on Chr. 22, also tumor suppressor function

17
Q

what are the S&S of neurofibromatosis?

A
  • Nodules along peripheral nerves
  • Axillary freckling, multiple café au lait spots, bony and connective tissue proliferation
  • Can cause an intracranial mass, most dangerous in brainstem and on cranial nerves
  • NF2 is specific to VIII nerve, and is bilaterally symmetrical
18
Q

dx and txt for neurofibromatosis

A

dx: part genetic, part PE
txt: surgery, if malignant transformation= chemo

19
Q

what are “honorary” CNS tumors?

A

Pituitary gland tumors (very common)
Sits below optic chiasm (in sella turcica, so growth tends to impinge central chiasm –> loss of affected retinal projections
-acromegaly from excess growth hormone

20
Q

affected retinal projections in honorary CNS tumor…

A

-Nasal fibers cross in anterior chiasm
Superiotemporal visual field loss for each eye (bitemporal hemianopsia)
-Macular fibers cross in posterior chiasm
Central scotomata (blind spot)

21
Q

main symptoms from CNS tumor are from…

A

mass effects- focal deficits, HA, seizures

22
Q

what are our particular pts in regards to CNS tumors?

A

Watch for at-risk patients with pseudotumor cerebri/IIH (obese women with headache and papilledema)