neuro 18 Flashcards

(32 cards)

1
Q

cardinal feature of toxic-metabolic encephalopathy

A

waxing and waning level of arousal; asterixis is a frequent finding

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2
Q

most common presentation of neurosarcoidosis

A

cranial neuropathy due to chronic basal meningitis, with facial and optic nerves most freq affected

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3
Q

pathology for neurosarcoidosis

A

noncaseating granuloma

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4
Q

treatment for neurosarcoidosis

A

steroids

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5
Q

neuropathy in DM

A

distal symmetric sensory polynuropathy; predilection for involvement of small myelinated and unmyelinated fibers; loss of temp and pinprick sensation

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6
Q

autonomic neuropathy in DM

A

gustatory sweating, orthostatic hypotension, diarrhea, and impotence

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7
Q

Whipple disease

A

dementia, seizures, myoclonus, ataxia, supranuc ophthalmoplegia, oculomasticatory myorhthmia

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8
Q

Wernicke’s encephalopathy triad

A

opthalmoplegia, truncal ataxia, and confusion; developing over a period of days to weeks

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9
Q

opthalmoplegia

A

weakness or paralysis of extraocular muscles

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10
Q

other manifestations of Wernicke’s encephalopathy

A

impaired pupillary light response; hypothermia; postural hypotension; and other evidence of nutritional def

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11
Q

what causes wernicke’s enceph

A

deficiency in thiamine

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12
Q

treatment for wernicke enceph

A

IV thiamine; ocular signs can resolve within hours and the confusion over days to weeks; the gait ataxia may persist

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13
Q

Korsakoff’s syndrome

A

isolated memory deficits that persist after Wernicke’s enceph; patients have confabulation

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14
Q

what causes subacute combined degernation of the spinal cord?

A

vit B12 def; degeneration of posterior (dorsal columns) and lateral white matter tracts of the SC

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15
Q

presentation of vit B12 def

A

insidious onset of paresthesias in the hands and feet; with time, weakness and spasticity develop in the legs;

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16
Q

what is elevated when B12 is deficient?

A

homocysteine and methylmalonic acid, the precursors of B12

17
Q

folate def

A

may cause the same def as in B12 but typically you see the heme def without the neuro

18
Q

characteristics of antiphospholipid syndrome

A

venous or arterial thrombosis; recurrent fetal loss; and thrombocytopena; this disease is assoc with elevated titers of antibodies directed against phosppholipids

19
Q

anti-phospholipid antibodies

A

in vitro prolongation of the PTT (lupus anticoagulant); can occur in isolation or in assoc with underlying immune disorder

20
Q

when to do a work up for anti-phospholipid antibody

A

young patients with stoke or in those with otherwise unexplained stroke; dx requires demonstration of high titer IgG antiphospholipid antibodies on two occasions

21
Q

treatment of anti-phospholipid antibody syndrome

A

warfarin to achieve INR between 3 and 4

22
Q

antiphospholipid antibody refers to what

A

it’s a general term that encompasses the lupus anti-coagulant, anticardiolipin antibodies, and antibodies against a mixture of various phospholipids

23
Q

nervous system is more commonly affected by hypo or hyperthyroidism

A

hypothyroidism

24
Q

central pontine myelinosis

A

rare demyelinating disorder that occurs most often in alcholics and may be precipitated b too-rapid correction of hyponatremia

25
clinical presentation of central pontine myelinosis
affects the pons and the basal gang, thalamus, and subcortical white matter; acute confusion, spastic quadriparesis, locked-in syndrome, dysarthria, and dysphagia
26
lumbosacral radiculoplexus neuropathy
asymm pain followed by weakness and atrophy in one leg
27
most common cause of lumbosacrak raduculoplexus neuropathy
type 2 DM, also occurs in type 1
28
hypothyroidism
assoc with entrapment neuropaties (carpal tunnel) or an axonal polyneuropathy
29
sarcoidosis
assoc with cranial neuropathies, a meningoencephalities, or hypothal dysfunction
30
weakness involving both the upper and lower face
dysfunction of the LMN
31
weakness that spares the forehead
dysfunction of UMN
32
causes of facial neuropathy
Lyme and sarcoidosis