7/28/16 Flashcards
what is the normal RBC to WBC ratio in CSF?
1 WBC to each 500-1000 RBCs
loss of all function (flaccid paralysis) except for position and vibratory sensation below a spinal cord level, loss of deep tendon reflexes
anterior spinal artery occlusion
ddx: position and vibratory sensation are lost, motor pain and temperature intact
subacute combined degeneration of the cord (B12 deficiency or neurosyphilis)
loss of pain and temperature on one side and loss of position and vibratory sense on the other side below a spinal cord level
brown-sequard syndrome (unilateral hemisection of sp cd)
presentation of tuberous sclerosis
RETINAL LESIONS, NEUROLOGICAL ABNORMALITIES (seizures, mental retardation), SKIN (leathery plaques on trunk, hypopigmented patches, reddened facial nodules), RENAL ANGIOMYOLIPOMAS, cardiac rhabdomyomas
port-wine stain on the face, seizures
sturge-weber syndrome
tx of mild vs severe parkinson disease
mild: ANTICHOLINERGICS (benztropine, trihexyphenidyl), AMANTADINE (in older pts intolerant of anticholinergics)
severe: DOPAMINE AGONISTS (pramipexole, ropinirole), LEVODOPA/CARBIDOPA, COMT INHIBITORS (extend duration of levodopa/carbidopa), MAO INHIBITORS (slow progression of disease)
what are the important side effects of the anticholinergic medications given to mild parkinson disease pts?
benzytropine and trihecyphenidyl cause dry mouth, WORSENING of PROSTATE HYPERTROPHY, and constipation
what are the important side effects of the medications given to severe parkinson disease pts?
levodopa/carbidopa are associated with “ON/OFF” phenomena, where insufficient dopamine can cause BRADYKINESIA (off), or too much dopamine can cause DYSKINESIA (on)
MAO inhibitors can cause hypertensive crisis if taken with tyramine-rich foods
pt with parkinson syndrome symptoms PLUS autonomic problems such as orthostatic hypotension, impotence, incontinence, dry mouth, dry skin
multiple system atrophy (Shy-Drager syndrome)
tx for dyskinesia of huntington disease
tetrabenazine
what should you consider in a pt with multiple sclerosis on chronic suppressive medication has worsening neurological deficits and MRI shows new, multiple white matter hypodense lesions
NATALIZUMAB is associated with development of PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY (PML)
what are the best drugs to prevent relapse in multiple sclerosis?
glatiramer and beta-interferon
tx for amyotrophic lateral sclerosis (ALS)
RILUZOLE (prevent progression), BACLOFEN (for spasticity)
what nerve affected: wasting of hypothenar eminence, pain in 4th and 5th fingers
ulnar nerve
what nerve affected: wrist drop
radial nerve (saturday night palsy = pressure on inner, upper arm; crutches)
what nerve affected: pain/numbness in ankle and sole of foot that worsens with walking
Tibial nerve (Tarsal Tunnel syndrome)
what nerve affected: weak foot with decreased dorsiflexion and eversion
peroneal (high boots, pressure on back of knee)
tx for guillain barre syndrome
IVIG OR plasmapheresis (NOT STEROIDS and NOT BOTH)
pathogenesis of myasthenia gravis and presentation
autoantibodies against acetylcholine receptors at the neuromuscular junction, presents in YOUNG WOMEN OR OLD MEN with ptosis, difficulty chewing, slurred speech, diplopia, weakness of limb muscles EXACERBATED BY CONTINUOUS USE
what imaging should be done in pts with confirmed myasthenia gravis?
chest CT with contrast to look for thymoma
tx for myasthenia gravis
neostigmine or pyridostigmine (acetylcholinesterase inhibitors)
distinguishing features of myasthenia gravis vs lambert-eaton syndrome
myasthenia gravis sx WORSEN with repeated muscle stimulation, whereas lambert-eaton syndrome (small cell lung cancer antibodies against presynaptic calcium channels) causes weakness that IMPROVES with repeated stimulation
management of myasthenia gravis pts that are refractory to medications
under 60 = thymectomy
over 60 = prednisone
tx for acute myasthenic crisis
IVIG or plasmapheresis