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69 Cards in this Set

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CNS/PNS
neuroectoderm
neural crest
mesoderm
NE: CNS, ependymal cells, oligodendroglia, astrocytes
NC: schwann cells, PNS neurons
M: microglia
Nissl substance (RER)
not in axons, but in dendrites & cell body
astrocytes
GFAP
bbb
reactive gliosis
Oligodendroglia
multiple CNS
fried eggs
MS
schwann cells
1 PNS axon
axonal regeneration
Guillain-Barre Syndrome
Acoustic neuroma
Free Nerve Endings
Meissner's corpuscles
Pacinian Corpuscles
Merkel's Disks
FNE: C, Aδ; all skin, epidermis, some viscera; pain and temp; unmyelinated; slow
MC: glabrous skin; dynamic fine touch; quick
PC: deep skin layers, ligaments, joints; vibration, pressure
MD: cup-shape, unencapsulated; hair follicles; static touch; slow
NE
DA
5-HT
ACh
GABA
NE: ↑anxiety, ↓depression; locus ceruleus
DA: ↑ schizo, ↓park.↓depression; ventral tegmentum, SNc
5-HT: ↓anxiety, depression; raphe nucleus
ACh: ↓Alz, Hunt., REM ↑park; basal nucleus of Meynert
GABA: ↓anxiety, hunt; nucleus accumben
HYPOTHALAMUS
SON
PVN
Lateral
VMA
Ant
Post
SN
SCN
SON: ADH
PVN: Oxytocin
Lateral: hunger; destroy=anorexia; (-)leptin
VMA: satiety; destroy=hyperphagia; (+)leptin
Ant: cooling, pArasym
Post: heat; SNS
DM: savage behavior & obesity
SN: sex urges
SCN: circadian rhythm & eye input
THALAMS
LGN
MGN
VPL
VPM
VA/VL
LGN: light=vision
MGN: music=hearing
VPL: body sensation (dorsal column, spinothalamic tract)
VPM: makeup=face (CN5)
VL/AL: motor
CEREBELLUM
mossy fibers/climbing fibers-->cerebellar cortex-->purkinje-->deep nuclei-->superior cerebellar peduncle-->output

vestibulocerebellum=folliculornodular+vermis-->fastigial (difficult balance, eye movment, medulloblastoma)
sphino cerebellum=vermis+paravermal-->fastigial+interpose (postural instability, slurred speech, pendulum knee jerks)
lateral cerebrospellum=lateral hemisphere-->dentate (no coordination, difficult control movement; termor extremitieis)

deep nuclei (L-->M: dentate, embliform/globose=interpose, fastigial)
parkinson
TRAP
Tremor rest
rigidity cogwheel
Akinesia, α-synuclein (lewy body)
Postural instability, shuffling gait, blank stare
depigment of substantia nigra pars compacta (loss of DA)
hemiballismus
contralateral subthalamic nucleus
huntington's
CAG repeat
Caudate loses ACh and GABA
Crazy
Chorea (BG lesion)
Chr4
Cuarenta y/o
enlarged lateral ventricles
asthestosis (snakelike)
pontine
affects smiling (CN7)
lateral vision (CN4)
amygdala (bilateral)
KLUVER BUCY syndrome
hyperorality
hypersexuality
disinhibited behavior
right parietal lobe
hemispatial neglect
(no makeup on 1 side of face)
L parietal lobe
gerstmann syndrome
agrafia
aclaculi
finger agnosia
L-R disorientation
RAS
reticular formation, locus ceruleus, raphe nucleus
arousal wakefulness
mammillary bodies
wernicke-korsakoff syndrome

COCA
confusion
ophthalmoplegia
confabulation
ataxia
BG
tremor at rest
chorea
athetosis
cerebellar hemisphere
cerebellar vermis
CH: intention tremor
limb ataxia; lateral location
ipsilateral

CV:
truncal ataxis
dysarthria
paramedian pontine reticular formation
eyes look away
frontal eye fields
eyes look toward lesion
superior calliculi
paralysis of upward gaze (paranaud syndrome)
central pontine myonosus
hypoNa+
irreversible
dysarthria
anterior spinal artery
medullary syndrome
contralateral hemiparesis
LE medial lemiscus
ipsilateral paralysis of CN12
pain & temp present
recurrent laryngeal
hoarseness
thyroidectomy
Weber syndrome
infarct paramedian branches of PCA
not occipital lobe
cerebral peduncle lesion: contralateral spastic paralysis
CN3 palsy (ipsilateral)
anterior communicating artery
posterior communicating artery
Ant: most common site of aneurysm
visual field defects

Post: aneurysm
CN3 palsy
posterior cerebral a.
PCA: visual cortex, macular sparing, medulla
lateral straite
arteries of stroke
pure motor emiparesis-->internal capsule, caudate, putamen, globus pallidus
charcot-bouchard microaneurymes
watershed zones
severe hypoTN
upper leg/upper arm weakness
defects in higher-order visual processing
AICA
face sensation and hearing loss ipsilateral
horner's
similar to PICA
LATERAL PONS
PICA
LATERAL MEDULLA
Wallenberg Syndrome
nystagmus
ipsilateral ataxia
n/v
horner's syndrome
lost pain/tmep
basilar artery
lock-in-syndrome
pons, midbrain, cerebrum
stroke of anterior circle
stroke of posterior circle
ANT: sensory and motor dysfunction
aphasia

POST: CN deficits
coma
cerebellar deficits
Epidural hematoma
Subdural hematoma
Subarachnoid hemorrhage
Parenchymal hematoma
bEla: biconcave, lucid, artery (middle menigeal); no suture line, cross falxtentorium
SDcgv: convex, gradual, veins, cross suture lines not falxtentorium
SA: worst hA; berryAneurysm, 2-3 days, vasospasm imodipine (red=acute, yellow=chronic by LP)
PH: htn, amyloid angiopathy, DM, tumor at lenticulate straie
ischemic brain disease
Hemorrhagic stroke
Ischemic Stroke
TIA
H: intracerebral bleed; aneurysm, 2⁰ ischemia, ↑fragility
I: emboli (a-fib, carotid dissection, patent foramen ovale, endocarditis) or lacunar strokes 2⁰htn; tPa 3hrs
TIA: brief, focal, reversible <24hrs
Ischmic Brain Disease imaging
dx.: CT-->ischemia
CT-->nothing-->hemorrhage (MRI) or <24hrs TIA

MRI: 3-30 mins bright for 10 days
CT: dark only after 24 hrs
Brain Ventricles
lateral ventricles
foramen of monroe
3rd ventricle
cerebral aqueduct/sylvius
4th ventricle
foramen of luschka(2) or magendie
subarachnoid
superior saggital sinus
Hydrocephalus
CT scan; reversible
triad: wacky (dementia), wet (urine incontinence), wobbly (gait problems)
nL/communicating: no absorption by arachnoid granulations (menigitis)
Obstruct/noncomun: block/stenosis
Hydrocephalus ex vacuo: ↑CSF atrophy
Pseudotumor cerebri: overweight young females, worst HA; papilloedema; ↑CSF pres, ↓outflow; nL ventricle; ; vitA, TCAs, OCPs; tx: acetalzolamide; no LP
Spinal tracts
Dorsal: pressure, proprioception, touch, vibration; medulla (gracilus in middle near penis)
Corticospinal: voluntary motor (legs lateral); medulla; anterior horn
Spinothalamic: (free nerve) pain, temp; anterior white commissure
UMN
LMN
U: ↑reflexes, ↑tone, babinksi, spastic paralysis, class knife spacitiy
L: ↓reflexes, ↓tone, atrophy, fasciculation,
poliomyelitis
werdnig hoffman disease
LMN lesions only
destroyed anterior horns-->flaccid paralysis
P: poliovirus fecal-oral; ↑lymphocytes
WH: AR, floppy baby, tongue fasciculations, botulism=honey
Multiple sclerosis
random, asymetric white matter lesions
autoimmune demyelination
SI3N
Scanning speech, Intention tremor, Incontinence, Internuclear opthalmoplegia, Nystagmus
↑IgG/protein, periventricular plaques, oligodendrocyte loss, preserved axons, oligoclonal bands
MRI: lesions of different ages (head, spinal cord)
tx: beta-interferon, cyclosporine, symptomatic
ALS
UPM, LMN lesion with signs
not affect sensory
SOD1
betel nut ingestion
Complete occlusion
spares dorsal column & tract of lissaue
upper thoracic: watershed area
artery of adamkiewicz: suppplies ASA below T8
Tabes Dorsalis
3⁰ syphillis: dorsal column, dorsal roots
charcot joints
shooting/lightening pain
APR
no DTRs
syringomyelia
damaged crossing fibers of spinothalamic tract (bilateral loss of pain & temp)
enlarged central canal
chaiari 2 malformation (C8-T1)
vit B12, vit E, Friederich's Ataxia
demyleination of dorsal columns,
lateral corticospinal tracts,
spinocerebellar tracts
ataxic gait, hyperreflexia, impaired position, vibration senses
FA: AR GAA, staggering, falling frat bro with pes cavus, hypertrophic cardiomyopathy, kyphoscoliosis, impaired mitochondrial functiong.all 4 limbs affected
Brown-Sequard syndrome
below T1
contralateral: spinothalamic
ipsilateral: corticospinal, dorsal column, loss all sensation
at level: LMN=flaccid paralysis
Horner's syndrome
PAM is horny
above T1
Ptosis
Anhidrosis
Miosis
ipsilateral compression of brachial plexopathy
pancoasts, brown-sequard syndrome, late-stage syringomyelia
cluster HA=partial
Nucleus Solitarius
Nucleus aMbiguus
Dorsal motor nucleus
NS: sensory (taste, baroreceptors, gut distention): CN7,9,10
NA: Motor pharynx, larynx, upper esophagus; CN9,10,11
DMN: autonomic (PNS) to heart, lungs, upper GI
Conductive HL
Sensorineural HL
C: BC>AC rinne; weber to affected ear
S: AC>BC rinne; weber to nL ear
Alzheimer's disease
cortical atrophy ↓ACh
senile plaques (β-amyloid)
abnL phosphorylated tau protein
down syndrome
chr1,14,19 (APOE4, AD), 21 (p-App gene)
Pick's Disease
frontotemporal dementia
intracellular, aggregated tau protein)
spares parietal lobe & post. 2/3 of superior temporal gyrus
Lewy Body Dementia
hallucinations + parkinsoniam
CJD
rapidly progressive
myoclonus
spongiform cortex
prions
Harono's
hippocampus eosinophilic Alzheimer's
Progressive Multifocal Leukoencephalopathy
Acute disseminated/postinfectious encephalomyelitis
Metachromatic Leukodystrophy
Charcot-Marie-Tooth Disease
PML: JC virus destroys oligodendrocytes; AIDS, rapid progressive, fatal
ADE: multifocal perivenular inflammation, demyelination (chickenpox, measles) or vaccinations (rabies, smallpox)
MLD: AR buildup of sulfatides (lysosomal storage disease) impairs myelin sheath production
CMTD: HMSN (hereditary); peripheral nerves of myelin affected
aids dementia
lipfoscin granules
herpes encephalitis
harono's
AD: multinucleated giant cells
LG: intranucleophile of aging & heart
HE: necrosis of temporal lobes
H: hippocampus eosinophilic alzheimer's
seizures
PARTIAL: 1 area
simple partial: conscious
complex partial: impaired
GENERAL: diffuse
absence/petit mal: blank stare
myoclonic: quick repetitive jerks
tonic-clonic/grand mal: alternate
tonic: stiff
atonic: drop (mistake for faint)
chlidren: genetic, infection, trauma, congenital, metabolic

adults: tumors, trauma, stroke, infection

elderly: stroke, tumor, trauma, metabolic, infection
HEADACHE
migraine
tension
cluster
M: 4-72hrs, light/noise; aura, pulsatile; CNV irritation; substance P; CGRP; vasoactive peptides
T: >30mins; bilateral
C: repetitive 4-8weeks; ipsilateral lacrimation; rhinorrhea; horner's males; tx O2
NEUROCUTANEOUS DISORDER
Sturge-Weber Syndrome
Tuberous Sclerosis
NF1 (vonRecklinghausen's disesase)
vHL disease
SWS: port-wine stain; ipsilateral leptomeningeal angioma; sporadic
TS: hamartomas; cardiac rhabdomyoma; renal angiomyolipoma; subependymal giant cell astrocytoma; MR; seizures; "ash leap spots" AD
NF1: cafe-au-lait spots; Lisch Nodules; neurofibromas AD chr17
VHL: delete VHL on chr3p AD; cavernous hemangiomas; RCC; hemangioblastoma
ADULT PRIMARY BRAIN TUMORS
Metastases: lung, breast, melanoma, RCC, GI
Glioblastoma multiforme (astrocytoma): #1; poor prognosis; butterfly glioma; GFAP; pseudopalisading
Meningioma: #2; spindle cells; psammoma bodies
Schwannoma: #3; CN8; S100; bilateral=NF2
Oligodendroglioma: fried egg calcification; chicken-wire capillary pattern
PituitaryAdenoma: prolactinoma; bitemporal hemianopa; hyper/hypopituitarism; rathke's pouch
CHILDHOOD BRAIN TUMORS
Pilocytic Astrocytoma: #1; well-circumscribed; GFAP; S100; rosenthal fibers; hair-like; cilial processes & microcysts; sometimes supratentorial
Medulloblastoma: #2; PNET; compress 4th ventricle; horner-wright rosettes
Ependymoma: #3; in 4th ventricle; perivascular pseudorosettes; rod shape blepharoplasts
Hemangioblastoma: vHL; polycythemia; foamy cells; highly vascularity
Craniopharyngioma: benign; bitemporal hemianopia; cholesterol cysts; calcification
HERNIATION
cingulate/subfalcine under falx cerebri
uncal
downward transtentorial/central herniation
cerebellar tonsillar herniation into foramen magnum
Uncal herniation
ipsilateral dilated pupil/ptosis=blown pupil
contralateral homonymous hemianopia
ipsilateral paresis (crus cerebri=kernohan's notch)
duret hemorrhages--paramedian artery rupture (caudal displace of brain stem)
Ring-enhancing lesion
Uniformly...
Heterogenitiy....
REL: toxoplasmosis; abscess, AIDs, metasteses, lymphoma
UEL: meningioma; lymphoma, metasese
HEL: glioblastoma multiforma