Case Studies Flashcards
55 yo male cc “foot drop”. weakness started 6 mon ago progressively worse, now involves thigh muscles of same limb.
Normal PE/Mental exam/ Sensory INTACT
CN2-12 shows slight dysarthria and furrowed tongue
Upgoing toe = +Babinski
HYPERREFLEXIVE
Amyotrophic lateral sclerosis (ALS) - crawls along spinal cord cephalad
Symmetric muscle weakness, sensory INTACT, increased CPK, HYPOREFLEXIVE
Polymyositis
Diplopia, ptosis, fatigue, extremity weakness is profound in neck flexors and proximal. Hallmark: first eye drop, double vision, can’t swallow. picks on midline first. NORMOREFLEXIVE.
weak, painless, sensory normal
Myasthenia Gravis
Which Nervous system (CNS or PNS) produces Hyperreflxive responses and which produces Hyporeflexive?
HYPER - CNS
HYPO - PNS
A child pre teen (5-12) is noted to have blank spells (staring) and no memory of the event. Pt remains awake but unable to interact. no aura.
MRI neg
EEG - 3hz spikes and slow wave discharge
Ethosuximide is prescribe with Excellent results.
What does this child have?
Juvenile Absence Epilepsy
A child (age 3-12) is noted to have episodes of brief muscle jerks (which he has amnesia for) esp when drowsy and occasional brief clonic seizures.
MRI neg
EEG shows a centro temporal spike with drowsiness
Benign Rolandic Epilepsy
age 3-12 issue brought on by sleep
no meds need child will grow out of problem
75 yo pt w/ prior hx of stroke notices foul smell then has a sense of nausea increasing from the stomach. Shortly after he falls and has tonic extension of limbs, then clonic shaking of limbs with bladder incontinence and biting of the side of his tongue. Cyanosis is noted followed by rapid breathing and awakening to a confused state
Focal seizure after stoke is common.
CT shows encephalomalacia
EEG shows phase reversing spike focus ipsilateral to the CVA
21 yo insulin dependent diabetic arrives in ED w/ hx clonic seizure. CT neg EEG pending EKG tacky low BP Lab - Glucose 35 urine ketones ++++
Hypoglycemic event assoc w/ excess insulin
this is a provoked seizure
*whenever giving glucose to an unconscious pt give 100mg thiamine first .
50 yo increasing gait instability and c/o muscle feeling stiff Exam normal, IQ normal Sensory INTACT, DTR normal Emotionless (bradykinesia) Rx trial (Sinemet) resolved symptoms
Parkinson’s
dementia and dysautonomia comes late in dz
80 yo w/ marked progressive (
Cortical Basilar Degeneration
Marked unilateral sx, rapid, refractory to Rx in older age onset
no tx available
21 yo w/ personality changes over 1 year and c/o involuntary movements. Father committed suicide but had progressive personality changes before.
Exam - chorea in UE, mood irritable and apathetic w/ mild cognitive slowing
Huntington’s Chorea
Early onset of personality changes, movement disorder w/ family hx
60 yo presents w/ rapid progressive gait instability
Exam: mild asymmetric muscle rigidity bradykinesia, nl DTR, nl sensory, no dementia.
Rx trial (Sinemet) did not work
MSA-p : Multiple system atrophy type P
rapid, refractory to meds, minimal dementia