Clin Med 2 Flashcards
Signs of neuromuscular jxn vs peripheral nerve problems vs muscle myositis
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
Signs of cerebellum ataxia. How is bil cerebellum is affected?
Ipsi ataxia w/o weakness, eye movement abnlities. By VZV —> immune system attacks both sides of cerebellum
Signs of Brown-Sequard syndrome
Ipsi motor weakness, contralat sensory, Ipsi DCML
arm fl>ex, leg ex>fl, sustained clonus, inc reflexes, spastic, memory change = sign of? Muscle fascicuations = sign of? Signs of motor neuron dz?
UMN sxs. LMN sxs. Mix of U/LMN sxs, involves 3+ limbs including head/face/tongue, progressive weakness, spastic, fasc, atrophy, cramps
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?
Brainstem. Spinal cord
aphasia vs naming (2nd order)
can’t produce or comprehend spoken/written lang vs ability to produce proper names of objects’ parts (2nd order)
clin features of parietal/sup MCA syndrome
all contralat hemiparesis/plegia, lower facial weakness, hemisensory loss, homonymous hemianopsia, Broca’s
anomic aphasia, Wern aphasia, amnesia, Kluver Bucy, contralat sup quadrantinopsia, visual/olf halluc
clin features of temporal/inf MCA syndrome
clin features of Gerstmann (special MCA)
acalculia, agraphia (can’t write despite know lang), finger agnosia, L/R confusion
clin features of acute internal carotid occlusion
contralat hemiplegia, lower facial weakness, homonymous hemianopsia, sensory deficit; mute, aphasia, dysarthria; eye dev towards lesion, ipsi Horner’s; cerebral edema
clin features of frontal lobe/ACA syndrome
contralat hemiparesis leg>arm; akinetic mute (no movements or speech, medial); dysarthria, transcortical motor aphasia; eye toward lesion; urin incont (medial), disinhibition
alexia w/o agraphia (can’t read but write), visual agnosia/Anton’s syndrome, optic apraxia/absent optokinetic nystagmus; contralat homonymous hemianopsia
clin features of occ lobe/PCA syndrome
how does CNS demyelinate?
T cells enter BBB –> macs come & eat myelin and axons –> demyelinated nerve fibers send signals slowly & irreg –> sclerotic/scarred plaques
risk factors of MS
females, Af-Am, teens to 40s, neuro impairment
what does CSF look like in MS?
inc markers in CSF v serum –> primary CNS inflamm; >2 oligoclonal bands, inc igG
optic neuritis sxs. how to eval? tx?
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