Clin Med 2 Flashcards

1
Q

Signs of neuromuscular jxn vs peripheral nerve problems vs muscle myositis

A

Diffuse weakness w/o sensory changes, worse/improving w/ exer, double vision vs numb/tingling, sensory changes; if there’s pain or dec reflexes —> radiculopathy/nerve root vs Proximal weakness, atrophy +/- pain, high CK & ESR

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2
Q

Signs of cerebellum ataxia. How is bil cerebellum is affected?

A

Ipsi ataxia w/o weakness, eye movement abnlities. By VZV —> immune system attacks both sides of cerebellum

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3
Q

Signs of Brown-Sequard syndrome

A

Ipsi motor weakness, contralat sensory, Ipsi DCML

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4
Q

arm fl>ex, leg ex>fl, sustained clonus, inc reflexes, spastic, memory change = sign of? Muscle fascicuations = sign of? Signs of motor neuron dz?

A

UMN sxs. LMN sxs. Mix of U/LMN sxs, involves 3+ limbs including head/face/tongue, progressive weakness, spastic, fasc, atrophy, cramps

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5
Q

If there are crossing of sxs, which structure should you think is affected? If you have urin retention or incont, which structure should you think is affected?

A

Brainstem. Spinal cord

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6
Q

aphasia vs naming (2nd order)

A

can’t produce or comprehend spoken/written lang vs ability to produce proper names of objects’ parts (2nd order)

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7
Q

clin features of parietal/sup MCA syndrome

A

all contralat hemiparesis/plegia, lower facial weakness, hemisensory loss, homonymous hemianopsia, Broca’s

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8
Q

anomic aphasia, Wern aphasia, amnesia, Kluver Bucy, contralat sup quadrantinopsia, visual/olf halluc

A

clin features of temporal/inf MCA syndrome

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9
Q

clin features of Gerstmann (special MCA)

A

acalculia, agraphia (can’t write despite know lang), finger agnosia, L/R confusion

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10
Q

clin features of acute internal carotid occlusion

A

contralat hemiplegia, lower facial weakness, homonymous hemianopsia, sensory deficit; mute, aphasia, dysarthria; eye dev towards lesion, ipsi Horner’s; cerebral edema

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11
Q

clin features of frontal lobe/ACA syndrome

A

contralat hemiparesis leg>arm; akinetic mute (no movements or speech, medial); dysarthria, transcortical motor aphasia; eye toward lesion; urin incont (medial), disinhibition

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12
Q

alexia w/o agraphia (can’t read but write), visual agnosia/Anton’s syndrome, optic apraxia/absent optokinetic nystagmus; contralat homonymous hemianopsia

A

clin features of occ lobe/PCA syndrome

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13
Q

how does CNS demyelinate?

A

T cells enter BBB –> macs come & eat myelin and axons –> demyelinated nerve fibers send signals slowly & irreg –> sclerotic/scarred plaques

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14
Q

risk factors of MS

A

females, Af-Am, teens to 40s, neuro impairment

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15
Q

what does CSF look like in MS?

A

inc markers in CSF v serum –> primary CNS inflamm; >2 oligoclonal bands, inc igG

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16
Q

optic neuritis sxs. how to eval? tx?

A

inflamm optic n, loss vision/color, pain w/ eye movement. ophthal eval: optic disc pallor; pupillary eval: afferent pupillary defect/Marcus Gunn pupil; VEP shows slowed conduction thru pupil; optical coherence tomography shows thick (acute) or thin (optic neuritis) retinal fibers. IV methylprednisolone

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17
Q

exec fxn vs attn vs agnosia vs apraxia

A

ability to organize, sequence, abstract info vs sel conc vs inability to recognize sensory input; occiptotemporal vs inability to carry out familiar actions; dom inf par lobe

18
Q

how does hippo vs amygdala contribute to mem?

A

spatial learning vs emotional mem

19
Q

cortical vs subcortical vs neurodegen amnesia w/ examples of each

A

changes in mem, lang, perception, fxn; temp, par, front. Alz, Lewy, vasc, frontotemporal dementia vs behavior, emotional, motor fxn, exec fxn; striatum, thal, midbrain. Parkinson, progressive supranuclear palsy, nml pressure hydrocephalus, CJakob dz, Huntington vs primary degen CNS dz. Alz, Lewy, frontotemporal dementia

20
Q

dementia w/u

A

H&P
Serum, UA, CBC w/ diff
folate, B12
Neuroimging: <65yo, <2y hx, focal neuro sxs, nml pressure hydrcephalus, trauma, neuropsych test

21
Q

examples of neuropsych testing

A

Mini Mental state Exam for mem & lang fxn
clock drawing test for visuospatial processing
“comb your hair”, “blow out match” for apraxia

22
Q

sxs of Alzheimers. chrm? gait?

A

dec mem & lang, disorientation, impaired reason/judge, decline in performing routine tasks. early = 1, 14, 21; late = APOE in 17. dementia-related gait changes –> dec in walking speed & stride, inc support phase; dual task-related gait changes –> in Alz & non-Alz dementia

23
Q

how to dx Alz? tx?

A

comprehensive hx, PE, labs, neuroimging of parietotemporal cortices; post mortem bx = definitive. cog enhancers (cholinesterase inhibitors, gluE antagonists), behavior (antipsychotics, antidepress, mood stabilizers, pain meds)

24
Q

carotid a dissection sxs. dx? tx?

A

HA, neck pain, ocular pain, partial Horner’s. duplex, CTA, MRA. anticoag w/ IV heparin, lovenox, ASA, plavix, tPA

25
Q

lacunar infarcts = caused by?

A

occlusion of deep penetrating aa

26
Q

brain venous infarct leads to?

A

venous congestion –> hemorrhagic changes

27
Q

arteriovenous malformation. tx?

A

abnl vessels b/w aa & vv w/o capillaries –> steals oxygenated blood –> hypoxic adjacent tissue –> axs, hemorrhage, sz. glue embolotherapy

28
Q

high altitude cerebral edema. tx?

A

going too high too fast –> vasogenic edema –> hypoxic cerebral vasodil –> capillary HTN, brain petechial bleed, CC edema –> atax, confusion, incont. acetazolamide, dexamethasone

29
Q

delirium confusion assessment method

A

presence of 1+2, or 3+4:
1. acute change in mental status
2. inattn
3. altered thinking
4. disorg thinking

30
Q

dementia

A

personality change, mem loss, impaired intellect from dz or trauma (NOT from age)

31
Q

Parkinson’s sxs vs dx vs tx

A

triad; bradykin, exec fxn, depression vs sensitive to psychotic & delirium meds –> must rule out before dx w/ dementia; Lewy in brainstem; DaT scan = sPECT scan w/ iodine labeling dopamine containing cells (not sensitive for early stage) vs dopamine/agonists, acetylcholine blockers (too much dopamine –> dyskinesia)

32
Q

Lewy body dementia. sxs?

A

Lewy bodies in brainstem, limbic system, cortex; can overlap w/ Alz or Park’s –> do PET to differentiate. visual halluc, abnl gait

33
Q

nml pressure hydrocephalus sxs vs dx vs tx. vasc dementia dx vs tx

A

wet, wobbly, wacky vs CT –> spinal tap vs shunt. MRI vs tx their HTN

34
Q

Creutzfeldt-Jakob dz

A

dementia, myoclonus, abnl EEG (periodic spikes) caused by prions. assoc w/ spongiform encephalopathy

35
Q

Wern vs Korsakoff. how to tx for both?

A

ocular, cerebellar, confusion, malnut vs anterograde, confab, malnut. IV thiamine, other B vit before B12

36
Q

AIDs. transient global amnesia. TBI. psychogenic amnesia

A

apathy, behavioral, cog decline, IVDU. antero/retrograde >50yo, temporal & spatial disorient, vasc insufficeny in midbrain. retrograde post fall/trauma. recent & remote mem loss, indifferent to deficits

37
Q

subdural hematoma. ca-related cog decline

A

fall, HA, lateralized sxs (hemianopsia, hemiplegia, CN abnlities). chemo + brain fog + weakness

38
Q

Huntington’s cause vs sxs vs tx

A

CAG rpt + loss cholinergic neurons in striatum –> GABA dec GPe to inc subthal to dec GPi –> inc thal –> inc movement vs dementia + chorea vs dopamine blockers for movement, bal dopamine & acetylcholine

39
Q

signs of unfavorable prog?

A

> 6cm, astrocytoma histo, cross midbrain, neuro deficits before resect

40
Q

hedgehog pathway

A

hedgehog make ligand to bind to PTCH –> initiates degradation –> SMO released –> activates Gli –> mostly for basal cell ca or medulloblastoma