neuro 18 Flashcards

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
Q

clinical presentation of central pontine myelinosis

A

affects the pons and the basal gang, thalamus, and subcortical white matter; acute confusion, spastic quadriparesis, locked-in syndrome, dysarthria, and dysphagia

26
Q

lumbosacral radiculoplexus neuropathy

A

asymm pain followed by weakness and atrophy in one leg

27
Q

most common cause of lumbosacrak raduculoplexus neuropathy

A

type 2 DM, also occurs in type 1

28
Q

hypothyroidism

A

assoc with entrapment neuropaties (carpal tunnel) or an axonal polyneuropathy

29
Q

sarcoidosis

A

assoc with cranial neuropathies, a meningoencephalities, or hypothal dysfunction

30
Q

weakness involving both the upper and lower face

A

dysfunction of the LMN

31
Q

weakness that spares the forehead

A

dysfunction of UMN

32
Q

causes of facial neuropathy

A

Lyme and sarcoidosis