pamhong-USMLE step 1 neuro

About this set

Created by:

pamhong  on April 13, 2012

Description:

Boards

Log in to favorite or report as inappropriate.
Pop out
No Messages

You must log in to discuss this set.

pamhong-USMLE step 1 neuro

high NE
anxiety
1/200
Preview our new flashcards mode!

Study:

Cards

Speller

Learn

Test

Scatter

Games:

Scatter

Space Race

Tools:

Export

Copy

Combine

Embed

Order by

Terms

Definitions

high NE anxiety
low NE depression
high DA schozphrenia
low DA parkinson's and depression
low seratonin anxiety and depression
low Ach Alzheimer's huntington, REM sleep
low gaba anxiety, huntington
glutamine + vit b6 GABA
NE synth location locus cerules/reticular formation/solitary tract
DA synth formation ventral tegmentum, SNc
seratonin synth location raphae nucleus
ACh synth location basal nucleus of meynert
GABA synth location nucleus accumbens
DA ptwy: mesocotical block ventral tegmentum of MB to cortex.
blocked: increase positive Sx of schizophrenia
Da ptwy: mesolimbic ventral tegmentum of MB to limbic system.
blocked: relief of pschosis (+Sx)
DA ptwy: nigrostriatal substantia nigra par compacta to striatum (caudate and putamen).
blocked: parkinson dz/ stimulation: extrapyramidal a/e
DA pwty: tuberoinfendibular: arcuate nucleus of hypoth to pituitary
blocked: increases prolactin- sx: amnorrhea, gynecomastia, galactorrhea
reticualr acivating system locus cerelus, reticular formation and raphae nuclei. Mediates cosciousness and alertness bc synth 5ht,NE. Damge: coma.
free nerve ending pain and temp.
a-delta and c-fiber
c-fibers free nerve ending. slow unmyelinated. warm temp
A delta fibers free nerver ending. fast, meylinated, cold temp
meissner's corpuscle large, meylinated. hairless skin (superficial skin)
position and dynamic touch
fast adapting
pacinan corpuscle lg, meylinated (deep skin), ligaments, joints. fast adapting
vibration and pressure
merckle's disk hair follicle.(superficial skin)/ slow adapting
position, static touch-edges, textures
ruffini encapsulated/ slow adapting/
deep layers. sole of foot
BBB composition 1. tight junctions b/w NON-fenestrated capillary endothelial cells (destruction- vasogenic edema)
2. BM 3. astrocyte processes
BBB permeability glucose and AA cross via carriers- slow
lipid-soluable and non-polar- fast via diffusion
non BBB, fenestrated capillaries in brain 1. area postrema- vomiting after chemo (CZT at medulla)
2. OVLT- osmotic sensing 3. neurosecretory products- ex: ADH
supra optic nucleus hypothalamus nuclei- makes ADH
paraventricular nucleus- hypothalamus nuclei- makes oxytocin
lateral area of hypothalamus FN- hunger. Inhibited by leptin
destructionn- anorexia, failure to thrive (infants)
zap lateral you shrink laterally
ventromedial area of hypothalamus FN- satiety. stimulated by leptin
destruction by craniopharyngioma- hyperphagia
zap ventromedial you grow ventral and medial
antetior hypothalamus cooling, parasymp.
A/C- anterior cooling
posterior hypothalamus heating, symp
suprachiasmatic nucleus circadian rhythm
thalamus: VPL input: spinothalmic / dorsal coums and medial lemniscus
info: pain and temp (from body)
output: primary somatosensory cortex.
thalamus: body sensation VPL
thalamus: VPM input: trigeminal and gustatory ptwy
info: face sensation and taste
output: primary somatosensory cortex
thalamus LGN input: CN II
info: vision
output: calcarine sulcus (occipital lobe)
thalamus: MGN input: superior olive and inferior colliculus of pons
info: hearing
output: auditory cortex (temporal lobe)
thalamus: communication w/ prefrontal cortex . damage? mediodorsal (MD) nucleus
dmaage: memory loss
thalamus: cerebellum (dentate n.) and basal ganglia VL
thalamus: VA basal ganglia to prefrontal, premotor, and orbital cortices
thalamus: anterior nuclear group mamillothalmic tract to cingulate gyrus
part of papez circuit
thalamus: pulvinar integration of vision, auditory, and somesthetic input
cerebellum input contralateral cortex via middle cerebellar peduncle
ipsilateral proprioception via inferior cerebellar peduncle
nerves: climbing and mossy fiber
cerebellum output contralateral cortex via superior cerebellar peduncle
nerves: purkinje fibers
modulates movement
spinocerebellum vermis and paravermis via fastigial and interposed nuclei
interposed n = globise and emboliform
vestibulocerebellum flocculonodular lobe and vermis via fastigial nuclei
cerebrocerebellum lateral hemispheres via dentate
cerebellum nuclei lateral to medial: dont eat greasy food
dentate, emboliform, globose, fastigial
lateral cerebellum voluntary movement of extremities
medial cerebellum balance, truncal coordination, ataxia
injury: ipsilateral - falls to injured side bc info crosses twice
basal ganglia: direct ptwy NT: dopamine receptor: D2R
SNc + , + striatum, - GPi, + thalamus = movement
basal ganglia: indirect ptwy NT: dopamine receptor D2R
+SNc, - striatum, +GPe, -Subthalmic n.& Gpi, +thalamus = movement
basal ganglia: GPi decrease/inh mov
basal ganglia: GPe inhibits STN and Gpi = increases movement
basal ganglia: STN stimulated GPi = inhibits movement
basal ganglia and PD loss of DA= less direct ptwy , more indirect ptwy = less motion
basal ganglia and HD neuronal death via NMDA-R : glutamate toxicity
atrophy of striatal nuclei (main inh of mov)
multiple sysmtem atrophy: parkison-like, autonomic dysFN, ataxia
inclusion w/ alpha synuclein in oligodendroglia cells
paramedian pontie reticular formation (PPRF) lesion eyes look away from lesion
frontal eye fields lesion eyes look towards lesion
cerebellar hemisphere lesion intention tremor, limb ataxia, ipsilateral
cerebellar vermis lesion TRUCAL ataxia, dysarthia
reticular activating system (MB) lesion reduced levels of arousal and wakefulness = coma
superior colliculi lesion paralysis of upward gaze
left parietal lobe lesion gerstman syndrome- agraphia, acalculia, finger agnosia, left and right disorientation
bilateral amygdale lesion kluber-bucy syndrome: hyperorality, hypersexuality, disinhited behavior
central pointine myelinosis acaute paralysis, dipliopia, loss consciousness.
bc rapid correction of HYPO-natremia
broca's aphasia nonfluent aphasia but understands
INFERIOR frontral gyrus
wernecke's apahsia fluent aphasia, but impaired comphrehension
SUPERIOR temporal gyrus
global apahsia nonfluent and impair comprehension. both broca and wernecke
conduction aphasia poor repetition. pt understands and is able to speak but no connection. At arcuate fasciculus
non-dominant broca aphasia expressive dysprosody- can't express emotions/inflection on speech "monotone"
non-dominant wernecke apahsia receptive dysprosody- inability to comphrehend emotion or inflectionin speech
weber's syndrome midbrain infarct occlusion of paramedian branches PCA
contralateral hemiparesis (CST) & oculomotors CN III palsy
CN 3 rostral midbrain.
levator palpebrae, superior, inferiorm, and medial rectus. inferior oblique/ pupillary sphincter- ciliary muscle
Cn 4 caudal midbrain- superior oblique
CN 6 caudal pons- lateral rectus
anterior spinal art contralat- hemiparesis (LE), ipsilateral paralysis of CN9
pain and temp are ok
PICA/ lateral medullary/wallenberg contralat- pain and temp in BODY
ipsilat- dysphagia, decrease gag reflex, dipliopia, nystagmus, horner's, facial tmep and pain, ataxia
AICA/ lateral inferior pontine synd ipsilateral facial paralysis (cn7), cochlear n. & nystagmus (cn8), facial pain & temp
PCA contralat- hemianopoa w/ MACULAR SPARING
MCA contralat- face, arm paralysis/sensation, apahsia(dominant), left side neglect (non-dominant)
ACA contralat- leg-foot motor and sensory
anterior communicating art MC site of berry aneurysm. visual problems- bitemporal hemianopsia
posterior communicating art CN 3 palsy- down and out
lateral striate from MCA. pure motor hemiparesis (arms & legs)
internal capsule, caudate, putamen, GP. "arteries of stroke"
watershed zone b/w ACA and MCA or MCA and PCA
HYPOtension,upper leg + arms weakness, high order visual process
basilar art locked in syndrome. only CN3 is intact!
aneurysm causes APKD, marfan, ehlers danlos
charcot bouchard microaneurysm ass w/ chronic HTN- small vessel in basal ganglia and thalamus
stroke at thalamus only sensory loss in cotralateral side both arms and legs. no motor defecit. but difficult to walk bc loss of proprioception
nimidipine CCB used after aneurysm to decrease risk of vasospam
parenchymal hematoma HTN, amyloid angiopathy- lobar stroke, DB, CA
at basal ganglia and internal capsule
intraventricular hemorrhage PREMES < 32 wks , low birth wgt < 1500
ischemic stroke emboli. a-fib, carotid dissection, patent foramen ovale, endocarditis, lacunar stroke-HTN.
cystic cavity w/ reactive gliosis.
TIA reversible. < 24 hrs
dural venous sinus superior sagital sinus (main location of CSF return) --> confluence of the sinus --> transverse sinus--> sigmoid sinus --> int. jugular v.
where does the sigmoid sinus become IJV jugular foramen
foramen of monro latreal ventricle to 3rd ventricle
cerebral aqueduct 3rd to 4th ventricle
CSF made in choroid plexus/ reabsorbe by choroid sinus
foramen of luschka 4th ventricle to subarachnoid space. LATERAL
foramen of magendie 4th ventricle to subarachnoid space. MEDIAL
normal pressure hydrocephalus wet, wobbly, wacky. NO increase in volume.
dementia, ataxia, urinary incontinence
pseudotumorcerebri young, obese female w/ daily HA worse in AM and papilledema
N- ventricles, no tumor/masses. but HIGH csf press.
tx- lose wgt, acetozolamide
fasciculus cuneatus dorsal column- upper extremities
fasciculus gracilis dorsal column- lower extremities. (more medial)
lateral CST arms are medial, legs are lateral
polio & werdnig hoffmann dz LMN lesion - destructoin anterior horns- flaccid paralysis
anterior spinal art and cord lose everything but dorsal columns and tract of lissauer. (proprioception, touch and temp ok)
3 syphilis DRG and dorsal column lesion
vit b12, vit E def, friedreich ataxia dorsal coumn, lateral CST, spinocerebellar tract
ataxia, hyperreflexia, impair vibration. ok temp & pain
polio CSF lymphocytic pleocytosis no protein.
SOD1 ALS- UMN and LMN
friedreich ataxia AR. repeat dz- GAA. frataxin protein. inpaired mitochondria. freq falling, nystagmus, dysarthia, hypertrophic CMP, kid- kyphoscoliosis. loss of CN8, 10, 12, cerebellum
brown sequad syndrome hemisecition.
ipsilateral- UMN. tactile, vibration, sensation, LMN
contralat- pain and temp below lesion
C2 posterior half of skull
C3 turtle neck shirt
C4 clavicle region. low collar shirt
T4 nipple
T7 xiphoid process
t10 umbiicus
L1 inguinal lig
L4 kneecaps "down in all fours"
S2,3,4 erection and sensation of penile and anal zone
reflex s1,2 achilles
reflex L3,4 patella
reflex C5.6 bicep
reflex C7,8 tricep
moro reflex "hang on for life" baby opens arms when thinks is falling backwards
CN that lie medial in brain stem CN 3-MB, CN 6- pons, CN 12- medulla.
CN 7 motor- facial mov, eyelid closing, stapedius muscle in ear
sensory- taste ant 2/3 tongue, lacrimation, salivation
Cn9 sensory- taste post 1/3 tongue, salivation-parotid, monitoring carotid body & sinus-chemo R
motor- swallowing, stylopharyngrus (elevates pharynx, larynx)
Cn 10 sensory- taste epiglottic region, aortic chemo & baro-R,
motor- palate elevation, midline uvula, talking, coughing
thoracoabd viscera
corneal reflex and lacrimation afferent- V1
efferent- cn 7
jaw jerk V3 sensory, v3 motor both via masseter
gag reflex cn9 afferent,
cn 9, 10 efferent
vagal nuclei: n. solitarius visceral sensation- taste, baro-R, ut distantion. CN 7,9,10
vagal nuceli: n. ambiguous motor innervation pharynx, larynx, upper esophagus- Cn 9, 10, 11
dorsal motor nucleus vagal nuclei. sends autonomic (parasymp) fibers to heart, lung, GI
ear: webber test turning fork in middle top head.
n- hear it on both ears = midline
conduction defect- ipsilateral
sensory defect = contralateral
ear: rinne test fork at mastoid then at ear.
N- AC>BC
conduction defect= AC<BC
ear: webber-R
Rinne LE: AC>BC, RE: BC>AC
R- webber--> R-conduction or L- sensory
rinne- LE ac>bc normal
rinne-RE bc>ac conduction
cavernous sinus CN 3,4,5 (V1, V2) ,6
internal carotid and post ganglionic symp
carvernous sinus syndrome ophthalmoplegio, ophthalmic and maxillary sensory loss
ass- w/ infections b/w nose and lip.
uvula deviation to the left 1. Cn 10 and nucleus ambiguous on the RIGHT
2. corticobulbal tract/motor cortex on the LEFT
tongue deviation to the left 1. Cn 12 Left
2. CBT / motor cortex on R
can't turn head to left, and should droop on R CN 11 on R.
palsy of lower face UMN lesion think of stroke.
upper face is innervated by both UMN so the ipsilateral UMN still functional
palsy entire half of face bell's palsy. damage at nuclei. LMN
causes of Bell's palsy Lovely Bella Had An STD
lyme, HSV, Aids, Sarcoidosis, Tumor, DB
bilateral bell's lyme dz, guillian barre
open angle glaucoma obstruction at canal of schlemn
slow, oainless, bilateral
close angle galucoma obstruction of flow from posterior to anterior chamber.
painful, acute, rock hard eye, frontal HA, halos, raindown around lights, non-reactive pupil
dont give EPI: miadriasis
cataracts/ congenital/ risk opacity of lens. / congenital- rubella
classical galactosemia, galactokinase def, DB
CN 4 damage eye drifts upward- vertical dipliopia
problems reading, going town the stairs
CN 6 damage medially directed eye
miosis pupilary pschincter muscle. parasymp Cn 3 from EW n. to ciliary ganglion.
mydriasis radial muscle, symp. T1 preganglionic- sup cervical ganglkion- postgl. symp- long ciliary nerve.
marcus gunn pupil damage in CN2. shine light in one eye- both dilated/ shine light on ok eye- both constrict. AFFERENT problem
macular degeneration dry vs wet loss of central vision.
dry- slow- fat deposits
wet rapid. neovascularization
damage to optic tract on R loss of right retina field.= loss of left visual field
homonymous hemianopia
damage to meyer's loop on R in temporal lobe
L upper quadrant anopia.
damage to dorsal optic radiation R parietal lobe MCA
L lower quadrantic lesion
INO lesion of MLF causes palsy of medial rectus (Cn3) when looking laterally. the normal eye moves laterally and has nystagmus.
both eyes goinward on accomodation.
alzheimers senile plaques: b-amyloid (dark cotton balls)
neurofibrillary tangles- TAU phosphorylation (flame shape)
pick's dz frontotemporal dementia
dementia, aphasia, change in personality
pick's body- ROUND tau, stains w/ silver
lewy body dementia parkinson w/ dementia, VISUAL hallucinations, repeated falls, and syncope.
alpha-synuclein defect (lewy body)
MS oligoclonal bands (IgG to oligodendroglia cells)
periventricular plaques
guillain barre' motor fibers. symmetric. ascending/ autonomic dysFN
CSF- high protien no WBC / papilledema
ass w/ campylobacter
PML AIDS+
JC virus - destruction of oligodentroglia
acute disseminated (post inf) encephalomyelitis multifocal inflamm and demyelination after infection. no necrosis. ass w/ kids and chickenpox/measles
metachromatic leukodystrophy AR lysosomal storage dz
arylsulfatase A def. - impair production of myelin
charcot marie-tooth dz hereditary- motor and sensory neuropathy
def in protein ass w/ meylin. - palpable perineal n. but thin calfs
constant demyelination/remyelination- onion bulb look
seizures general 1. absence- 3hz, no postictal confusion- blank stare
2. myoclonic- jerks
3. tonic-clonic- grand mal. stiff and jerks
4. tonic- stiff
5. atonic- drop. mistaken for fainting.
simple vs comple sz simple- consciousness is intact.
complex- impaired consciousness
causes if sz by age kids- genetic>inf>trauma
adults- tumors>trauma>stroke>inf
elderly- stroke> tumor>trauma>metabolic>inf
cluster HA unilatral. brief HA. every day for several wks
tearing, runny nose! horner's
tx/; O2 +/- sumitriptan
tension HA bilateral. > 30 mins. dull pain no othe associated sx
frontal-occipital region
migraine unilatreal- pulsating, n/v, photophobia, phonophobia, possible aura. tx: sumitriptan for acute/ BB for prophylaxis.
trigeminal neuralgia lightening pain, electrical shock like w/ min stimuli- bed sheets, wind.
tx- carbamezepine,
sturge webber syndrome cong. port wine stain at trigeminal region (V1)
ipsilateral letomeningeal angioma
pheochromocytoma
tuberous sclerosis hamartomas in CNS, cadiac rhabdomyomas
renal angiolypomas. ashleaf spots
Von Hipple Lindau dz cavernous hemangiomas in skin, mucosa
BILATERAL renal cell CA- increases epo
pheocrhomocytoma, hemangioblastoma in cerebellum
GMB MC 1 tumor adults GFAP+ / pesudopalisading cells
hemispheres. crosses corpus callosum. / necrosis.
meningioma 2nd MC in adults
whorled pattern. psammoma bodies - calcification rings
schwannoma 3rd MC in adults. resectable S-100 +
bilateral aucustic schwannoma - NF2
oligodendroglyoma slow growing. frontal lobes. GFAP +
fried eggs cells and chicken wire capillary
pilocytic astrocytoma kids. GFAP + usually at cerebellum - cyst and solid
rosenthal fibers- eosinophilic corckscrew fibers
medulloblastoma cerebellar tumors kids. PNET
homer-wright rosettes. small blue cell Ca
epndymoma at 4th ventricle. kids. hydrocephalous.
perivascular pseudorosettes.(white area around BV)
hemangioblastoma kids. cerebellum w/ foamy cells. ass w/ vHL syndrome.
produces EPO- 2nd polycythemia
craniopharyngioma benign kids. from rathke's pouch- calcification- enamel like
bitemporal hemianopsia.
uncal herniation ipsilateral- CN 3 palsy, paresis( compression crus cerebri-contralat)
contralateral- homonymous hemianopia (comp ipsilat PCA)
cingulate herniation subfalcine. under falx cerebri.
compression ACA
downward transtectorial herniation compression cerebral aqueduct- hydrocephalus
cerebellar tonsil herniation into foramen magnum
ass w/ arnol chiari

First Time Here?

Welcome to Quizlet, a fun, free place to study. Try these flashcards, find others to study, or make your own.

Set Champions

There are no high scores or champions for this set yet. You can sign up or log in to be the first!