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501 Cards in this Set

  • Front
  • Back
CNS neurons origin
neuroectoderm
ependymal cells origin
neuroectoderm
oligodendrocytes origin
neuroectoderm
astrocytes origin
neuroectoderm
schwann cells origin
neural crest
PNS neurons origin
neural crest
microglia origin
mesoderm
permanent cells
neurons
do not divide in adulthood
where is nissl substance located and what is it?
in cell body of nucleus
RER
astrocytes function
5
physical support
repair
K+ metab
removal of excess neurotransmitter
maintain blood brain barrier
reactive gliosis in response to injury is done by what type of cell?
astrocyte
what cell type maintains the blood brain barrier?
astrocyte
astrocyte marker
GFAP
CNS phagocytes- what type of cell?
microglia
HIV infected microglia form what in the CNS?
multinucleated giant cells
each oligodendrocyte myelinates how many axons?
up to 30 each
white matter in the CNS is made of what type of cell
oligodendrocyte
what cells are destroyed in MS
oligodendrocytes
what CNS cells look like fried eggs on H&E
oligodendrocytes
how many axons do schwann cells myelinate?
1
what type of cell is destroyed in guillain barre?
schwann cells
what cells are responsible for axonal regeneration?
schwann cells
what type of tumor is an acoustic neuroma? where is it located?
schwannoma
located in internal auditory meatus- CN 8
free nerve endings:
what type of fibers
location
what do they sense
C, A-delta fibers
skin/epidermis/some viscera
pain and temp
meissner's corpuscles
location?
senses?
glabrous (hairless) skin near surface
dynamic fine touch, manipulation
pacinian corpuscles
location?
senses?
deep skin, ligaments, joints
vibration and pressure
(looks like onion)
Merkel's disks
location?
senses?
hair follicles
static touch, shape, edges, texture
endoneurium
invests single nerve fiber
perineurium
permeability barrier
surrounds fascicle of nerve fibers
what peripheral nerve layer must be rejoined in microsurgery for limb reattachment?
perineureum
epineureum
dense connective tissue that surrounds entire nerve (fascicles and blood vessels)
location of NE
locus ceruleus
location of dopamine
ventral tegmentum
SNc
location of seratonin
raphe nucleus
location of ACh
basal nucleus of meynert
locus ceruleus
NE
raphe nucleus
5HT
ventral tegmentum
dopamine
SNc
dopamine
basal nucleus of meynert
ACh
NT changes in anxiety
increased NE
decreased 5HT
NT changes in depression
decreased NE
decreased 5HT
NT changes in schizophrenia
increased dopamine
NT changes in parkinsons
decreased dopamine
NT changes in Alzheimers
decreased ACh
NT changes in Huntingtons
decreased ACh
decreased GABA
blood brain barrier is formed by what 3 structures?
1. tight junctions between nonfenestrated capillary endothelial cells
2. basement membrane
3. astrocyte foot processes
what crosses BBB slowly via carrier mediated transport?
glucose
amino acids
what crosses BBB rapidly via diffusion?
lipids
region of brain with fenestrated capillaries and no BBB?
area postrema (vomit after chemo)
OVLT (osmotic sensing)
neurohypophysis (neurosecretory products are released into circulation)
Name 2 other blood barriers besides the blood brain barrier
1. blood-testis
2. maternal fetal blood barrier of placenta
vasogenic edema can be caused by
infarction destroying endothelial cell tight junctions (disrupts BBB)
Hypothalamus functions:
TAN HATS
Thirst
Adenohypophysis control
Neurohypophysis releases its hormones
Hunger
Autonomic regulation
Temperature regulation
Sexual urges
OVLT
inputs to hypothalamus
senses changes in osmolarity
inputs to hypothalamus
OVLT- osmolarity changes
area postrema- respond to emetics
Name 8 parts of the hypothalamus
supraoptic nucleus
paraventricular nucleus
lateral
ventromedial
anterior
posterior
septal nucleus
suprachiasmatic nucleus
supraoptic nucleus
part of HT
makes ADH
what makes ADH
supraoptic nucleus of HT
paraventricular nucleus
part of HT
makes oxytocin
what makes oxytocin
paraventricular nucleus of HT
lateral area of HT
hunger
what happens if you destroy the lateral area of the HT?
anorexia
what inhibits the lateral area of HT?
leptin
what part of HT causes hunger?
lateral area
ventromedial area of HT
satiety
destruction of ventromedial area of HT causes what?
hyperphagia
what part of HT causes satiety?
ventromedial area
what stimulates the ventromedial area of HT?
leptin
what does leptin inhibit? what does leptin stimulate?
lateral HT
ventromedial HT
Anterior hypothalamus
cooling
parasympathetic
posterior hypothalamus
heating
sympathetic
septal nucleus of hypothalamus
sexual urges
what part of the brain regulates sexual urges
septal nucleus of HT
what part of HT regulates cooling, parasympathetic function?
anterior
(A/C think cold!)
what part of HT regulates heat, sympathetic function?
posterior
suprachiasmatic nucleus
part of HT
circadian rhythm
circadian rhythm location
suprachiasmatic nucleus of HT
posterior pituitary function
receives HT axonal projections from supraoptic (ADH) and paravenricular (oxytocin)
thalamus function
major relay for ascending sensory information
major relay for ascending sensory information?
thalamus
lateral geniculate nucleus of thalamus
vision (light)
medial geniculate nucleus of thalamus
sound (m for music)
ventral posterior nucleus, lateral part
VPL
part of thalamus
body sensation
ventral anterior/lateral nuclei (VA/VL)
part of thalamus
motor
ventral posterior nucleus, medial part VPM
part of thalamus
facial sensation
blood supply to thalamus
posterior communicating
posterior cerebral
anterior choroidal arteries
limbic system- 4 parts
cingulate gyrus
hippocampus
fornix
mammillary bodies
limbic system function
5 Fs
feed
fight
flee
feel
sex
middle cerebellar peduncle
cerebellum
contralateral cortical input
inferior cerebellar peduncle
cerebellum
ipsilateral proprioceptive input
cerebellum inputs
middle cerebellar peduncle- contralat
inferior cerebellar peduncle- ipsilat
types of input nerves of cerebellum
climbing and mossy fibers
type of output fibers of cerebellum
Purkinje fibers
superior cerebellar peduncle
output to contralateral cortex via purkinje fibers
deep nuclei of cerebellum
(from lateral to medial)
Dentate
emboliform
globose
fastigial
(dont eat greasy foods)
lateral deep nuclei of cerebellum
dentate is most lateral
then emboliform

movement of extremities
medial deep nuclei of cerebellum
globose
fastigial

truncal coordination, balance
basal ganglia function
voluntary movement
postural adjustment
basal ganglia input is from
cortex
basal ganglia feeds back to
cortex
SNc - substantia nigra pars compacta
dopamine 1 and 2
D1
excitatory
D2
inhibitory
striatum is made up of
caudate
putamen
caudate
part of striatum of basal ganglia
cognitive
putamen
part of striatum of basal ganglia
motor
excitatory pathway of basal ganglia
SNc dopamine binds D1
stimulates motion
inhibitory pathway of basal ganglia
SNc dopamine binds D2
inhibits motion
basal ganglia:
stimulatory
cortex stimulates striatum
thalamus stimulates cortex
STN stimulates GPi (which inh thal)
basal ganglia:
inhibitory
striatum inhibits GPi
GPi inhibits thalamus

striatum inhibits GPe
GPe inhibits STN (which stim GPi which inh thalamus)
globus pallidus externus
inhibits the STN from stimulating GPi to inhibit the thalamus.

Sooo you get motion (thalamus is NOT inhibited)
globus pallidus internus
inhibits the thalamus
striatum:
direct excitatory pathway
indirect inhibitory pathway
inhibits the GPi = motion

inhibits the GPe (which stimulates STN/GPi) = no motion
parkinson's features
degenerative
Lewy bodies- alpha synuclein
depigmentation of substantia nigra
parkinson's symptoms
tremor at rest
cogwheel rigidity
postural instability

TRAP
MPTP
contaminant of illicit street drugs that has been linked to parkinsons
lewy bodies
parkinsons
alpha synuclein
alpha synuclein
lewy bodies
parkinsons
substantia nigra
parkinsons
hemiballismus
what is it?
where is the lesion?
flail 1 arm
contralateral subthalamic nucleus
(STN can no longer stimulate GPi to inhibit the thalamus)
Hungtingtons genetics
AD
trinucleotide repeat CAG
chromosome 4
huntingtons mechanism
atrophy of caudate nucleus
loss of GABA neurons and ACh
leads to enlarged lateral ventricles
huntingtons symptoms
chorea
progressive dementia
middle aged
depression
athetosis
chorea
what is it
where is lesion
jerky purposeless movement
caudate nucleus of basal ganglia
athetosis
what is it
where is the lesion
slow writhing, esp fingers
snakelike
caudate of basal ganglia
essential or postural tremor
action tremor
autosomal dominant
self medicate with alcohol
treat essential/postural/action tremor
beta blocker
resting tremor
parkinsons
(pill rolling)
intention tremor
slow zigzag motion when pointing
cerebellar dysfunction
executive functions
frontal lobe
medial homunculus
leg
lateral homunculus
arm/face
motor aphasia
good comprehension
brocas lesion
fluent speech
poor comprehension
wernickes lesion
conduction aphasia
good comprehension
fluent speech
poor repetition
arcuate fasciculus
hyperorality
hypersexuality
disinhibited behavior
kluver-bucy syndrome
amygdala- bilateral lesion
spatial neglect syndrome
agnosia of contralateral world
right parietal lesion
reduced levels of arousal and wakefulness
reticular activating system- midbrain
confusion
confabulation
ophthalmoplegia
ataxia
wernicke korsakoff
mammillary bodies- bilateral
rest tremor
chorea
athetosis
basal ganglia lesion
intention tremor
limb ataxia
cerebellum
(fall towards side of lesion)
truncal ataxia
dysarthria
cerebellum vermis
contralateral hemiballismus
subthalamic nucleus lesion (basal ganglia)
anterograde amnesia
hippocampus lesion
Paramedian pontine reticular formation lesion
eyes look away from the side of the lesion
frontal eye field lesion
eyes look toward the lesion
aphasia
higher order inability to speak
dysarthria
motor inability to speak
anterior cerebral artery
leg
middle cerebral artery
trunk, arm, face
brocas
wernickes
visual cortex artery
posterior cerebral artery
most common site of circle of Willis aneurysm
anterior communicating artery
location of aneurysm causing CN III palsy
posterior communicating artery
infarct of what causes pure motor hemiparesis
internal capsule
stroke arteries
lateral striate- divisions of MCA
(caudate, internal capsule, putamun, globus pallidus)
severe hypotension damages what areas?
watershed areas
between ACA and MCA or PCA and MCA
wallenberg syndrome artery
PICA infarct
nystagmus
ipsilateral ataxia
nausea
vomiting
Horners
wallenberg syndrome
PICA infarct
locked in syndrome artery
Basilar artery
general sensory and motor dysfunction
aphasia
stroke of anterior circle
vertigo
visual field defects
coma
ataxia
stroke of posterior circle
berry aneurysms location
bifurcation in circle of willis, Anterior communicating artery
berry aneurysm rupture causes
subarachnoid hemorrhage
berry aneurysms are associated with what 3 diseases
adult polycystic kidney disease
ehlers danlos
marfans
charcot brouchard aneurysms
microaneurysms
chronic HTN
small vessles- basal ganglia, thalamus
epidural hemorrhage cause
middle meningeal artery
secondary to fracture of temporal bone
subdural hematoma cause
rupture of bridging veins
venous bleeding
subdural hematoma is seen in these 4 cases
elderly
alcoholics
blunt trauma
shaken baby
crescent shaped hemorrhage that crosses suture lines
subdural hematoma
biconvex hemorrhage that does NOT cross suture lines
epidural hematoma
subarachnoid hemorrhage cause
rupture of an aneurysm or AVM
bloody or yellow (xanthochromic) spinal tap
subarachnoid hemorrhage
type of bleed associated with HTN, amyloid angiopathy, DM, tumor

typical location?
parenchymal hematoma

basal ganglia, internal capsule
hemorrhagic stroke
intracerebral bleeding
often due to aneurysm rupture
may be secondary to ischemic stroke following reperfusion
ischemic stroke
emboli blocking large vessel
causes of ischemic stroke: 4
atrial fib
carotid dissection
PFO
endocarditis
lacunar strokes
block small vessels,
secondary to HTN
TIA
brief reversible episode
focal ischemia
less than 24 hrs
stroke imaging:
bright on ? in what amount of time
dark on ? in what amount of time
MRI in 3-30 min
CT in 24 hours
venous sinuses run where?
dura mater, where meningeal and periosteal layers

cerebral veins-> venous sinuses-> IJV
main location of CSF return via subarachnoid granulations
superior sagittal sinus
lateral ventricle to 3rd via what?
foramen of monroe
3rd ventricle to 4th ventricle via what?
aqueduct
4th ventricle to subarachnoid granulations via what?
foramen of luschka- lateral
foramen of magendie- medial
hydrocephalus
accumulation of excess CSF in ventricular system--> increased intracranial pressure and ventricular dilation
dementia
gait problems
urinary incontinence
triad of hydrocephalus

(wet, wobbly, wacky)
normal pressure communicating hydrocephalus
inpaired absorption of CSF by arachnoid granulations

post meningitis arachnoid adhesions
obstructive noncommunicating hydrocephalus
stuctural blockage of CSF in ventricular system

stenosis of aqueduct
hydrocephalus ex vacuo
increased CSF in atrophy
normal intracranial pressure
how many spinal nerves?
31
how many cervical nerves
8
how many thoracic nerves
12
how many lumbar nerves
5
how many sacral nerves
5
how many coccygeal nerves
1
nerves C1-C7 exit via
intravertebral foramina above corresponding vertebra

(all others exit below)
normal location of vertebral disk herniation
between L5 and S1
(nucleus pulposus herniates through annulus fibrosus)
adults, spinal cord extends to
L1-L2
subarachnoid extends to
lower border of S2
lumbar puncture is performed where?
L3-L4 or L4-L5 interspaces
at level of cauda equina
to keep the cord alive, keep the spinal needle between
L3 and L5
landmark for lumbar puncture
iliac crest
order of structures pierced in lumbar puncture: 7
1. skin/superficial fascia
2. ligaments (supraspinous, inter, ligamentum flavum)
3. epidural space
4. dura mater
5. subdural
6. arachnoid
7. subarachnoid space- CSF
what is not pierced in lumbar puncture
pia
fasiculus cuneatus
arms- dorsal column
fasiculus gracilis
legs- dorsal column
dorsal column artery
posterior spinal arteries (2)
lateral corticospinal tract- what is medial and what is lateral
medial- arms
lateral- legs
what is in the intermediate horn?
sympathetics- thoracic cord only
spinothalamic tract- what is lateral?
legs
sacral sparing
dorsal column 1st order neuron
cell body in DRG
ascends ipsilaterally
DC synapse 1
ipsilateral nucleus cuneatus or gracilis
DC 2nd order neuron
decussates in medulla
ascends contralaterally in medial lem
DC synapse 2
VPL thalamus
DC 3rd order neuron
sensory cortex
ST 1st order neuron
A-delta and C fibers- cell body of DRG
ST synapse 1
ipsilateral gray matter
ST 2nd order neuron
decussates at anterior white commissure

ascends contralaterally
ST synapse 2
VPL thalamus
ST 3rd order neuron
sensory cortex
Lateral CST 1st order neuron
UMN:
cell body in primary motor cortex
descends ipsilaterally thru internal capsule
lateral CST decussates
caudal medulla (pyramids)
lateral CST synapse 1
cell body of anterior horn of spinal cord
lateral CST 2nd order neuron
LMN:
leaves spinal cord
lateral CST synapse 2
neuromuscular junction
atrophy is what type of motor neuron sign
LMN
fasciculations are what type of motor neuron sign
LMN
anterior horn lesion
polio
werdnig hoffmann
random white matter lesions
MS
anterior horn lesions and lateral CST lesions
ALS
ASA occlusion spares what?
dorsal columns
dorsal column lesions
tabes dorsalis- syphilis
anterior commissure lesion
syringomyelia
dorsal column and lateral CST lesions
vitamin b12 deficiency
friedreichs ataxia
LMN destruction only
polio
werdnig hoffman floppy baby
CSF with lymphocytic pleocytosis with slight elevation of protein and normal glucose
polio
floppy baby
werdnig hoffman disease
tongue fasciculations in baby
werdnig hoffman disease
infantile spinal muscular atrophy
werdnig hoffman disease
genetics of werdnig hoffman disease
AR
both LMN and UMN findings
ALS
defect in superoxide dismutase 1 (SOD1)
ALS
degeneration of dorsal columns and dorsal roots
tabes dorsalis
tertiary syphilis
impaired proprioception
locomotor ataxia
charcots joints
shooting pain
absence of DTRs
tabes dorsalis
argyll robertson pupils
tabes dorsalis
they accomodate but do not react
staggering gait
frequent falling
nystagmus
dysarthria
hypertrophic cardiomyopathy
childhood kyphoscoliosis
Friedreich's ataxia
Friedreich's ataxia genetics
AR
trinuc repeat GAA
frataxin gene
--> imparied mitochondria
brown sequard
hemisection of spinal cord
1. ips UMN
2. ips DC
3. contralat ST
4. ips sensation at level of lesion
5. LMN at level of lesion
lesion above T1
horners
horners
ptosis
anhidrosis
miosis
ptosis
eyelid drooping
miosis
pupil constricts
anhidrosis
lack of sweating
lesions causing horners
brown sequard
pancoasts tumor
late stage syringomyelia
horners pathway
3 neuron oculosympathetic:
HT->
intermediolat column of spinal cord->
superior cervical ganglion->
pupil, smooth muscle of lid, sweat glands
pudendal nerve block (pregnancy) landmark
ischial spine
appendix landmark
mcburneys
2/3 from umbilicus to anterior superior iliac spine
lumbar puncture landmark
iliac crest
C2
back of skull
C3
high turtleneck
C4
low collar shirt
T4
nipple
T7
xiphoid
T10
umbilicus
L1
inguinal ligament
L4
knee
S2,S3,S4
penile/anal zones
biceps reflex
C5 nerve root
triceps reflex
C7 nerve root
patella reflex
L4 nerve root
achilles reflex
S1 nerve root
muscle spindle
muscle stretch->
Ia afferents ->
alpha motor neuron ->
reflex contraction
muscle spindle helps you monitor
muscle length
golgi tendon monitors
tension (drop heavy suitcase)
gamma loop
contracts intrafusal fibers ->
increase sensitivity of muscle spindle reflex arc
moro reflex
startle baby->
extend limbs
rooting reflex
stroke baby's mouth or cheek-->
turn head

(nipple seeking)
sucking reflex
touch roof of baby's mouth->
sucking
palmar (and plantar) reflex
stroke baby's palms ->
curl fingers
medial cranial nerves
3,6,12
pineal gland
melatonin
circadian rhythm
superior colliculi
conjugate vertical gaze
inferior colliliculi
auditory
parinaud syndrome
paralysis of conjugate vertical gaze due to lesion of superior colliculi
lesion of superior colliculi
parinaud syndrome- paralysis of conjugate vertical gaze
submandibular and sublingual glands
CN ?
7
parotid gland CN ?
9
eyelid closing CN ?
7
eyelid opening CN ?
3
monitoring carotid body and sinus chemo and baroreceptors
CN ?
9
CN that elevates pharynx and larynx
9 (thru the stylopharyngeus)
(10 does palate elevation)
taste from epiglottic region
CN?
10
CN that elevates palate
10
monitoring aortic arch chemo and baroreceptors
CN ?
10
midbrain cranial nerves
3,4
pons cranial nerves
5,6,7,8
medulla cranial nerves
9,10,11,12
lateral nuclei
sensory or motor
sensory
medial nuclei
sensory or motor
motor
corneal reflex
afferent
efferent
V1
7
lacrimation reflex
afferent
efferent
V1
7
jaw jerk reflex
afferent
efferent
V3 sensory
V3 motor
pupillary reflex
afferent
efferent
2
3
gag reflex
afferent
efferent
9
9,10
nucleus solitarius
visceral sensory
7,9,10
nucleus ambiguous
motor- larynx, pharynx, upper esoph
9,10,11
dorsal motor nucleus
autonomic (para) to heart/lungs/GI
cribiform plate
1
optic canal
2
opthalmic artery
central retinal vein
superior orbital fissure
3,4, V1, 6
foramen rotundum
V2
foramen ovale
V3
foramen spinosum
middle meningeal artery
internal auditory meatus
7,8
jugular foramen
9,10,11
jugular vein
hypoglossal canal
12
foramen magnum
spinal roots of 11
brain stem
vertebral arteries
cavernous sinus nerves
3,4, V1,V2, 6
postganglionic sympathetic fibers
internal carotid artery

6 is free floating
ophthalmoplegia
ophthamlic and maxillary sensory loss
cavernous sinus syndrome due to mass effect
sella turcica and diaphragma sella surround the
pituitary
hypothalamus is next to what ventricle
3rd
what sinus is inferior to the the pituitary
sphenoid sinus
what sinus is lateral to the pituitary
cavernous
CN 12 lesion- tongue deviates
towards lesion
CN V motor lesion- jaw deviates
towards lesion
CN 10 lesion- uvula deviates
away from lesion
CN 11 lesion- shoulder droop
on side of lesion
contralateral paralysis of lower face
UMN lesion
ipsilateral paralysis of upper and lower face
LMN lesion
peripheral ipsilateral facial paralysis
inability to close ips eye
bells palsy
bell's palsy
destruction of facial nucleus or efferent fibers causing ipsilateral paralysis
bells palsy is seen in:
6
AIDS
Lyme
Herpes
Sarcoid
Tumors
DM
test palate elevation
kuh kuh kuh
(10)
test tongue
la la la
(12)
test lips
mi mi mi
(7)
muscles that close the jaw
masseter
temporalis
medial pterygoid
muscles that open jaw
lateral pterygoid
mastication muscles innervated by
V3
muscles with glossus
CN 12
except palatoglossus (10)
muscles with palat
CN 10
(except tensor veli palatini- V3)
glaucoma
impaired aq humor flow->
increased pressure ->
optic disk atrophy
open angle glaucoma
obstructed outflow, canal of schlemm
silent, painless
african american, older, myopia
closed angle glaucoma
obstruction behind iris, lens
painful
decreased vision
DONT GIVE EPI
cataract
painless
opacification of lens
decreased vision
age, smoke, alchohol, DM, infection
papilladema
increased intracranial pressure
elevated optic disk
blind spot
test inferior oblique
IOU
look up (and in)
test superior oblique
look down and in
strabismus
misalignment of eyes
amblyopia
reduction of vision from disuse in critical period
miosis muscles
pupillary sphincter muscle
parasympathetic
miosis- pupillary sphincter innervation
CN 3 from Edinger Westphal to ciliary ganglion
mydriasis muscles
radial muscle/pupillary dilator muscle
sympathetic
mydriasis- pupillary dilator innervation
T1 preganglionic symp->
superior cervical ganglion->
postganglionic sympth->
long ciliary nerve
pupillary light reflex pathway
light-> CN 2->
pretectal nuclei of midbrain ->
EW nuclei ->
lateral geniculate nuclei->
ciliary gangion ->
pupillary constrictor muscles
Marcus Gunn pupil
afferent pupillary defect
shine light in affected eye, decreased bilateral pupil constriction
CN 3 output to ocular muscles is primarily affected by
vascular diseases (DM)
CN 3 parasympathetic output is affected by
compression (aneurysm, herniation)
retinal detachment
separation of neurosensory layer of retina from epithelium->
degeneration of photoreceptors->
vision loss
causes of retinal detachment
DM
trauma
age-related macular degeneration
degeneration of central area of retina
scotoma
dry ARMD (age related mac degen)
slow, gradual dec in vision
wet ARMD (age related mac deg)
rapid
due to neovascularization
MS
autoimmune demyelination of CNS (brain and SC)
optic neuritis (sudden loss of vision)
internuclear opthalmoplegia
nystagmus
hemiparesis
bladder incontinence
MS
increased protein/IgG in CSF
MS
periventricular plaques
MS
(areas of oligodendrocyte loss and reactive gliosis with preservation of axons)
oligodendrocyte loss
preservation of axons
MS
MS epidemiology
women in 20s and 30s
treat MS
beta interferon
Guillain barre
demyelination of peripheral nerves and motor fibers of ventral roots

symmetric ascending muscle weakness (distal lower extrem)
facial paralysis in what percentage of guillain barre
50%
ascending muscle weakness
cardiac probs
HTN or hypotension
Guillain barre
mechanism of guillain barre
autoimmune attack of peripheral myelin due to molecular mimicry
treat guillain barre
IV immune globulins
plasmapharesis
increased CSF with normal cell count:
what is this called and what disease
albuminocytologic dissociation
guillain barre
albuminocytologic dissociation
high protein, normal or low cell count
guillain barre
increased protein in CSF
papilledema
PML
demyelination of CNS due to destruction of oligodendrocytes
JC virus
Acute disseminated postinfectious enceophalomyelitis
demyelination after infection or vaccine
metochromatic leukodystrophy
AR
lysosomal storage disease
arylsulfatase A deficiency
inc sulfatides-> damage myelin sheath
charcot marie tooth
motor and sensory
progressive hereditary
defective protein production involved with myelin sheath
4 demyelinating diseases (not guillain barre or MS)
1. PML
2. ADE (acute dissem encephalomyelitis)
3. Metachromatic leukodystrophy
4. charcot marie tooth
seizure caused by
synchronized, high frequency neuronal firing
partial seizure
1 area of brain
usual mesial temporal
simple partial seizure
consciousness is ok
complex partial seizure
impaired consciousness
generalized seizures
diffuse:
1 absence
2 myoclonic
3 tonic clonic
4 tonic
5 atonic- fall to floor
children causes of seizures
genetic
infection
trauma
congenital
metabolic
adult causes of seizures
tumor
trauma
stroke
infection
elderly causes of seizures
stroke
tumor
trauma
metabolic
infection
headache
pain due to irritation of dura or cranial nerves or extracranial
(not brain parenchyma)
migraine
unilateral
pulsating
nausea
light sensitive
up to 3 days
migraine causes- what nerve and what is released?
irritation of CN V
release of sub P and CGRP and vasoactive peptides
tension headache
bilateral
greater than 30 minutes
cluster headache
repetitive
brief
men
unilateral
periorbital
ipsilateral lacrimation, rhinorrhea
horners- ispilateral
vertigo
illusion of movement
peripheral vertigo
more common
inner ear cause- debris, infection
Menieres disease
positional test- delayed horizontal nystagmus
delayed horizontal nystagmus with positional testing
peripheral vertigo
central vertigo
brain stem or cerebellar lesion
postitional test- immediate nystagmus in any direction
immediate nystagmus with positional testing
central vertigo
sturge weber
congenital
port wine stain
ipsilateral leptomeningeal angioma
glaucoma
seizures
hemiparesis
MR
MR
hemiparesis
seizures
glaucoma
port wine stains
leptomeningeal angioma
sturge weber
tuberous sclerosis
CNS and skin hamartomas
cardiac rhabdomyoma
renal angiomyoliopoma
subepend giant cell astrocytoma
MR
seizures
ash leaf spots
tuberous sclerosis genetics
AD
ash leaf spots
tuberous sclerosis
angiomyolipoma
tuberous sclerosis
subependymal giant cell astrocytoma
tuberous sclerosis
hamartomas of CNS and skin
tuberous sclerosis
NF1
cafe au lait spots
lisch nodules- iris
NF1 genetics
AD
cafe au lait spots
NF1
lisch nodules
NF1
von hippel lindau
cavernous hemangiomas
renal cell carcinoma
hemangioblastoma in retina/brainstem/cerebellum
von hippel lindau genetics
AD
cavernous hemangioma
von hippel lindau
renal cell carcinoma and neurocutaneous disorder
von hippel lindau
retinal hemangioblastoma
von hippel lindau
brain stem/cerebellar hemangioblastoma
von hippel lindau
4 neurocutaneous disorders
sturge weber
tuberous sclerosis
NF1
von hippel lindau
cingulate/subfalcine herniation
under falx cerebri
compress ACA
downward transtentorial central herniation
down through tentorium cerebelli
uncal herniation
stretch CN 3
compress ipsilateral PCA
compress kernohans notch
duret hemorrhages- paramedian artery rupture
signs of uncal herniation
ipsilateral ptosis
ipsilateral dilated pupil
contralateral homonymous hemianop
ipsilateral paresis
uncal herniation-
what causes ipsilateral dilation of pupil/ptosis
CN3 stretches
(levator palpebrae)
uncal herniation-
what causes contralateral homonymous hemianopia
compress PCA
uncal herniation-
what causes ipsilateral paresis
compression of contralateral crus cerebri (kernohan's notch)
uncal herniation-
what causes duret hemorrhage
caudal displacement of brain stem-- paramedian artery ruptures
perilymph
inner ear, in the bony labyrinth
Na+ rich
parts of the inner ear
cochlea
vestibule
semicircular canals
endolymph
inner ear, in the membranous labyrinth
K+ rich
cochlear parts
cochlear duct
vestibule parts and function
utricle
saccule

detect linear acceleration
semicircular canal parts and function
ampullae

detect angular acceleration
cochlear membrane parts and what frequency sounds do they detect?
narrow base- high frequency
wide apex- low frequency
conductive hearing loss
bone conduction > air conduction on Rinne

Weber localizes to affected ear
sensorineural hearing loss
air conduction > bone conduction on Rinne

Weber localizes to normal ear
hearing loss in elderly
high frequency -> low frequency
layers of the eye in the back
sclera- white
choroid
retina
fovea
layers of the eye in the front
sclera- white
cornea
iris
lens
posterior chamber of the eye
behind iris, in front of lens
canal of schlemm
collects aqueous humor from trabecular meshwork which absorbs it
anterior chamber of eye
aqueous humor
what innervates lateral rectus
6
what innervates superior oblique
4
what does the superior oblique do?
abducts
intorts
depresses
eye looks down and out
ptosis
pupillary dilation
loss of accommodation
CN 3 damage
diplopia with downward gaze
CN 4 damage
medially directed eye
CN 6 damage
right optic nerve lesion
right anopia
optic chiasm lesion
bitemporal hemianopia
right optic tract lesion
left homonymous hemianopia
right Meyer's loop lesion (temporal lobe)
left upper quadrantic anopia
right dorsal optic radiation lesion (right parietal lobe)
left lower quadrantic anopia
lesion at the right calcarine fissure (end of the optic radiations)
left hemianopia with macular sparing
macular lesion (central retina)
central scotoma (macular degeneration)
internuclear opthalmoplegia
MLF syndrome
lesion in the medial longitudinal fasciculus -> medial rectus palsy on attempted lateral gaze
nystagmus in which eye with MLF syndrome/internuclear opthalmoplegia
abducting eye
MLF syndrome is commonly seen in what disease
MS
Look left with a normal MLF- what are the steps?
look left
left nucleus of CN 6 fires
contracts left lateral rectus
stimulates contralateral (right) MLF
stimulates right nucleus of CN 3
contracts right medial rectus
Look left with a damaged right MLF- what happens?
right beating nystagmus in left eye
medial rectus palsy in right eye
majority of adult primary brain tumors are located where?
supratentorial
majority of childhood primary brain tumors are located where?
infratentorial
most common primary adult brain tumor
glioblastoma multiforme
glioblastoma multiforme is what type of tumor
grade 4 astrocytoma
Bad prognosis
butterfly glioma
glioblastoma multiforme crossing corpus callosum
stain for glioblastoma multiforme astrocytes
GFAP
pseudopalisading cells
(pleomorphic near areas of necrosis and hemorrhage)
glioblastoma multiforme
2nd most common adult brain tumor
meningioma
meningiomas arise from
arachnoid cells
spindle cells arranged in whorled pattern
meningioma
psammoma bodies- laminated calcifications
meningioma
prognosis of meningioma
good?, resectable
3rd most common adult brain tumor
schwannoma
(acoustic)
bilateral schwannomas found in ?
NF2
prognosis for schwannoma
good
rare, slow growing, less common adult brain tumor
oligodendroglioma
oligodendrogliomas are often found where?
frontal lobe
chicken-wire capillary pattern
oligodendroglioma
fried egg cells of CNS
oligodendrocytes
Most common type of pituitary adenoma
prolactinoma
bitemporal hemianopia-causing tumor
pituitary adenoma
5 adult brain tumors:
1. GM
2. meningioma
3. schwannoma
4. oligodendroglioma
5. pituitary adenoma
5 childhood brain tumors:
1. pilocytic astrocytoma
2. medulloblastoma
3. ependymoma
4. hemangioblastoma
5. craniopharyngioma
well circumscribed low grade childhood tumor
pilocytic astrocytoma
posterior fossa
Rosenthal fibers- eosinophilic corkscrew fibers
pilocytic astrocytoma
highly malignant childhood tumor
medulloblastoma
form of PNET- primitive neuroectodermal tumor
medulloblastoma
childhood tumor that often compresses the 4th ventricle and causes hydrocephalus
ependymoma
(medullo can do this too)
rosettes
medulloblastoma
childhood tumor that is radiation sensitive
medulloblastoma
childhood tumor most commonly found in 4th ventricle
ependymoma
poor prognosis
2 childhood tumors with poor prognosis
ependymoma
medulloblastoma
pseudorosettes
ependymoma
rod shaped blepharoplasts- basal ciliary bodies
ependymoma
location of hemangioblastoma
retina/brain stem/cerebellar
seen in von hippel lindau
childhood tumor associated with von hippel lindau and retinal angiomas
hemangioblastoma
tumor that produces EPO and can cause secondary polycythemia
hemangioblastoma
foamy cells
hemangioblastoma
benign childhood tumor confused with pituitary adenoma
craniopharyngioma
most common childhood supratentorial tumor
craniopharyngioma
tumor derived from rathke's pouch remnants, commonly calcified
craniopharyngioma