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440 Cards in this Set

  • Front
  • Back
free nerve endings are present in all ___ and some ___
they sense ___ (2)
2 kinds are ___
skin
viscera
pain
temperature
Adelta
C
Adelta fibers are ___ (2)
fast
myelinated
Meissner corpuscles are present in ___
they sense ___ (2)
they are attached to ___ fibers
glabrous skin
fine touch
position
Abeta
Pacinian corpuscles are present in ___ (3)
they sense ___ (2)
they are attached to ___ fibers
another structure with the same functional charateristics is ___
deep skin layers
ligaments
joints
vibration
pressure
Abeta
Ruffini ending
Merkel disks are present in ___
they sense ___ (2)
they are attached to ___ fibers
hair follicles
static touch
position
Abeta
NE is ___ in depression, ___ in anxiety
it is made in ___
low
high
locus ceruleus
DA is made in ___ (2)
ventral tegmentum
SNc
5-HT is ___ in depression, ___ in anxiety
it is made in ___
low
low
raphe nuclei
ACh is ___ in Alzheimer's, ___ in Huntington's, ___ in REM sleep
it is made in ___
low
low
high
nucleus basalis of Meynert
GABA is ___ in anxiety, ___ in Huntington's
it is made in ___
low
low
nucleus accumbens
___ (2) cross BBB by carrier-mediated transport
Glc
amino acids
___ molecules cross BBB by diffusion
nonpolar
ADH is made in HTh ___ nucleus
supraoptic
oxytocin is made in HTh ___ nucleus
paraventricular
leptin acts on ___ HTh to block hunger and on ___ HTh to cause satiety
lateral (inhibitory)
ventromedial (stimulatory)
loss of ___ HTh causes failure to thrive
lateral
loss of ___ HTh causes hyperphagia
this can be caused by ___
ventromedial
craniopharyngioma
___ HTh nucleus heats the body in reponse to cold by boosting ___ tone
posterior
SYM
___ HTh nucleus cools the body in reponse to heat by boosting ___ tone
anterior
PARA
___ HTh nucleus drives sexual urges
septal
___ HTh nucleus drives circadian rhythm
suprachiasmatic
posterior pituitary receives projections from ___ (2) HTh
supraoptic
paraventricular
MGN of thalamus receives ___ info
auditory
VPLN of thalamus receives ___ info
via ___ (2) tracts
somatosensory from body (touch, pain, proprioception, etc)
spinothalamic
dorsal columns
VPMN of thalamus receives ___ info
via ___ (2) tracts
somatosensory for face
trigeminal discriminative touch
trigeminothalamic
motor region of thalamus is anterior/posterior
anterior
3 parts of limbic system
cingulate gyrus
hippocampus
amygdala
cerebellum receives ipsilateral input via ___ cerebellar peduncle
inferior
cerebellum receives contralateral input via ___ cerebellar peduncle
middle
cerebellum sends output via ___ cerebellar peduncle
superior
cerebellar output pathway
purkinje cells
deep nuclei
cortex (via superierior CP)
lateral cerebellum controls ___
limbs
medial cerebellum controls ___
gait
balance
2 motor control pathways from basal ganglia (BG)
direct
indirect
direct BG pathway is driven by ___ (2)
DA tone at striatum D1Rs
Glu tone at striatum
Glu tone at striatum is from ___
cortex
indirect BG pathway is driven by ___ and inhibited by ___
Glu tone at striatum
DA tone at striatum D2Rs
direct BG pathway:
striatum stimulates/inhibits ___
which stimulates/inhibits ___
which stimulates/inhibits ___
inhibits
GPi/SNr
inhibits
thalamus
stimulates
cortex
indirect BG pathway:
striatum stimulates/inhibits ___
which stimulates/inhibits ___
which stimulates/inhibits ___
which stimulates/inhibits ___
which stimulates/inhibits ___
inhibits
GPe
inhibits
STN
stimulates
GPi
inhibits
thalamus
stimulates
cortex
loss of DA in PD causes shift of tone to ___ pathway
this causes ___ of movement
indirect
inhibition
2 pathological changes in PD
depigmentation of SNc
Lewy bodies
Lewy bodies are made of ___
alpha synuclein
___ is a street drug contaminant which can cause parkinsonism
MPTP
lacunar stroke in ___ causes hemiballismus
STN
(why not GPi also?)
Huntingtons is a ___ trait linked to Chromosome ___.
AD
4
neurotoxicity in Huntington's is because of ___ from ___
excitotoxicity
Glu at NMDAR
Huntington's is caused by expansion of ___ repeats.
<= ___ repeats is normal
>= ___ repeats causes disease
CAG (Q)
27
36
chorea is caused by ___ lesions
BG
athetosis is caused by ___ lesions
BG
essential tremor is worsened by ___
it is improved by ___
it is txed with ___
maintaining a posture
alcohol
beta blockers
intention tremor is caused by ___ lesions
cerebellar
motor homonculus from inferolateral to superomedial (6)
larynx
face (inferior to superior)
hand (radial to ulnar)
arm (distal to proximal)
trunk (proximal to distal)
leg (proximal to distal)
lesion in amygdala causes ___ (3)
hyperorality
hypersexuality
disinhibition
(Klüver-Bucy syndrome)
frontal lobe lesions cause ___ (2)
disinhibition
problems with attention
bilateral mamillary body lesions cause ___ (4)
confusion
ophtalmoplegia
memory loss
ataxia
(Wernicke-Korsakoff syndrome)
lesions in PPRF cause ___ gaze deviation
contralateral
lesions in frontal eye field cause ___ gaze deviation
ipsilateral
too fast correction of hyponatremia causes ___
central pontine myelinolysis
in broca's aphasia ___ is intact
comprehension
in wernicke's aphasia ___ is intact
word pronunciation
in global aphasia ___ is intact
nothing (both broca's & wernicke's areas affected)
in conduction aphasia ___ is intact
comprehension
speech production
in conduction aphasia ___ is impaired
it is caused by lesion of ___
repetition
arcuate fasciculus
medial medullary syndrome is caused by ___
Sx are ___ (3)
basilar or vertebral artery occlusion
contralateral hemiparesis
contralateral deep hypoesthesia
ipsilateral hypoglossal palsy
hypoglossal palsy in medial medullary syndrome
causes ___lateral tongue deviation
ipsi
lateral medullary syndrome is caused by ___
it is aka ___ (2)
occlusion of posterior inferior cerebellar a.
PICA syndrome
Wallenberg syndrome
5 symptoms of lateral medullary syndrome
contralateral pain/temp hypoesthesia
ipsilateral facial pain/temp hypoesthesia
ipsilateral Horner's syn
ipsilateral nucleus ambiguus symptoms
vestibular sx
3 nucleus ambiguus sx
dysphagia (CN9)
hoarseness (CN10)
reduced gag reflex
4 vestibular sx
nystagmus
vertigo
vomiting
diplopia
lateral pontine syndrome is aka
AICA syndrome
5 sx of lateral pontine syndrome
contralateral pain/temp hypoesthesia
ipsilateral facial hypoesthesia
ipsilateral facial palsy
ipsilateral vestibulocochlear sx
ipsilateral ataxia
lateral pontine syn facial hypoesthesia includes ___ and ___
pain/temp
light touch
lateral pontine syn facial palsy includes ___ and ___
mastication
facial expression
lateral pontine syn vestibulocochlear sx
nystagmus
hearing loss
PCA strokes cause ___ visual deficit with ___
homonymous hemianopia
macular sparing
most common site of circle of Willis aneurysm
anterior communicating a.
ant. communicating a. lesions cause ___
visual field defects
post communicating a. aneurysms cause ___
CN3 palsy
lateral striate a.s are branches of ___
they perfuse ___ (2)
MCA
striatum
internal capsule
stroke in ___ causes pure motor hemiparesis
posterior limb of internal capsule
ischemia to watershed zones happens in severe ___
it presents as ___ (2)
hypotension
upper arm/leg weakness
high level visual processing defects
occlusion of ___ causes locked in syn
basilar
3 genetic diseases associated with berry aneurysms
Ehler-Danlos
ADPKD
Marfan's syn
Charcot-Bouchard aneurysms cause ___ associated with ___
BG hemorrhage
HTN
epidural hematomas are ___ shaped
they are/aren't contained by dural folds
lentil
aren't
subdural hematomas are ___ shaped
they are/aren't contained by dural folds
crescent
are
4 causes of parenchymal hemorrhage
HTN
amyloid angiopathy
DM
tumor
2 most common sites of parenchymal hemorrhage
BG
internal capsule
4 regions most vulnerable to ischemia
hippocampus
neocortex
cerebellum
watershed regions
5 stages in infarction
red neurons
neutrophilic infiltration
MQ infiltration
reactive gliosis
glial scar
red neurons are present after ___ hours
12-48
neutrophilic infiltration happens at ___ days
1--3
MQ infiltration happens at ___ days
3--5
reactive gliosis happens at ___ weeks
1--2
ischemic strokes can convert to hemorrhagic because of ___
increased vessel fragility
a stroke appears ___ on diffusion MRI after ___ hours
it remains that way for ___ days
and ___ on CT after ___ hours
bright
.05--.5
10
dark
24
dural sinuses empty into ___
internal jugular vein
main location of CSF return is into ___
sup. sagittal sinus
5 sinuses which meet at the confluence of sinuses
superior sagittal
L+R transverse
occipital
straight
straight sinus is fed by ___ (2)
inf. sagittal sinus
great vein of Galen
communicating hydrocephalus is caused by ___
reduced CSF return at arachnoid granulations
NPH has elevated ___
sx are ___ (3)
it is a kind of ___ hydrocephalus
ventricular volume
dementia
ataxia
incontinence
communicating
ICP in NPH is ___
high normal
hydrocephalus ex vacuo is caused by ___
brain atrophy
spinal nerves ___ exit via IV foramen above corresponding vertebra
spinal nerves ___ exit via IV foramen below corresponding vertebra
___ is a freak
C1-C7
T1-12, S1-5, Co
C8
C8 spinal nerve exits above ___
T1
IV disk most commonly herniated
L5-S1
SC usually extends to ___
subarachnoid space extends to ___
LP is performed at ___ or ___
L1-L2
S2
L3-L4
L4-L5
7 layers pierced in LP
skin
fascia
supraspinous ligament
interspinous ligament
ligamentum flavum
dura
arachnoid
fibers for legs are medial/lateral in corticospinal tract
lateral
fibers for legs are medial/lateral in lateral spinothalamic tract
lateral
fibers for legs are medial/lateral in dorsal columns
medial
soma of 1' neuron of dorsal column tract pathway is in ___
it terminates proximally in the ___lateral ___ or ___
DRG
ipsilateral
nucleus cuneatus
nucelus gracilis
decussation of dorsal column pathway is in the ___
medulla
decussation of dorsal column pathway is done by ___ neuron
2'
soma of 1' neuron of spinothalamic tract pathway is in ___
it terminates proximally in the ___lateral ___
DRG
ipsilateral
substantia gelatinosa
decussation of spinothalamic tract is done by ___ neuron
2'
decussation of spinothalamic tract is in the ___
anterior white commisure (SC at level of entry)
2 causes of pure LMN disease
polio
Werdnig-Hoffman disease
Werdnig-Hoffman disease is aka ___
infantile SMA
Werdnig-Hoffman disease is a ___ trait
it presents as ___ with ___
median life expectancy is ___
AR
floppy baby
tongue fasciculation
7 months
syringomyelia typically affects cord levels ___
it is associated with ___
C8-T1
arnold-chiari II
in arnold-chiari I ___ herniates
in arnold-chiari II, ___ herniates
___ is associated with myelomeningocele
cerebellar tonsils
cerebellar tonsils + medulla
arnold-chiari II
syringomyelia disrupts ___ tract at ___
spinothalamic
anterior white commisure
B12 deficiency affects ___ (3) tracts
same lesions can be caused by ___
dorsal columns
spinocerebellar
lateral corticospinal
Vit E deficiency
Friedreich's ataxia
poliovirus is transmitted by ___ route
it replicates in ___
fecal-oral
oropharynx
small intestine
5 non-neurological polio sx
headache
fever
nausea
abdominal pain
sore throat
3 CSF findings in polio
lymphocytosis
moderate protein elevation
normal glucose
2 causes of ALS
SOD1 mutation
betel nut
tabes dorsalis is caused by ___ syphilis
___ reflexes are lost
___ pupils are present
tertiary
deep tendon
Argyll Robertson
Argyll Robertson pupils are sensitive to ___ but not ___
accomodation
light
hemisection of the SC above T1 causes ___
Horner's syn
Horner's syndrome is caused by a lesion in ___ pathway
oculosympathetic
first neuron in oculosympathetic pathway is in ___ and ends in ___
HTh
intermediolateral colum of T1
second neuron in oculosympathetic pathway is in ___ and ends in ___.
IML column of T1 SC
superior cervical ganglion
diaphragm and gallbladder pain can be referred to ___ by ___ n.
right
phrenic
xiphoid process dermatome
T7
inguinal ligament dermatome
L1
kneecaps ligament
L4
penis dermatomes
S2-3
ankle jerk is from ___ cord levels
S1-2
knee jerk is from ___ cord levels
L3-4
biceps reflex is from ___ cord levels
C5-6
triceps reflex is from ___ cord levels
C7-8
___ is superior to superior colliculi
pineal gland
lesion of superior colliculi causes ___
this is called ___
it can be caused by ___
upgaze palsy
Parinaud syn
pinealoma
afferent arm of gag reflex is via CN ___
9
efferent arm of gag reflex is via CN ___
9 and 10
3 medullary vagal nuclei
NTS
ambiguus
dorsal motor
NTS processes ___ info from CNs ___
SVA + GVA
7
9
10
part of NTS which receives input from CN7
gustatory nucleus
nucleus ambiguus processes ___ info for CNs ___
SVE + GVE
9
10
11
dorsal motor nucleus processes ___ info for CNs ___
it controls ___
GVE
10
vagal tone to heart, lungs and upper GIT
cribriform plate transmits ___ from ___ to ___ through ___
olfactory nerve
anterior cranial fossa
nasopharynx
ethmoid bone
optic canal transmits ___ (3) from ___ to ___ through ___
optic nerve
ophthalmic a.
central retinal v.
middle cranial fossa
orbit
sphenoid bone
superior orbital fissure transmits ___ (6) from ___ to ___ through ___
oculomotor n.
trochlear n.
ophthalmic division of trigeminal n.
abducens n.
ophthalmic vein
sympathetic fibers
middle cranial fossa
orbit
sphenoid bone
foramen rotundum transmits ___ from ___ to ___ through ___
maxillary division of trigeminal n.
middle cranial fossa
pterygopalatine fossa
sphenoid bone
foramen ovale transmits ___ from ___ to ___ through ___
mandibular division of trigeminal n.
middle cranial fossa
infratemporal fossa
sphenoid bone
foramen spinosum transmits ___ (2) from ___ to ___ through ___
middle meningeal a.
meningeal branch of mandibular n. (nervus spinosus)
middle cranial fossa
infratemporal fossa
sphenoid bone
internal auditory meatus transmits CNs ___ and ___ from ___ through ___
7
8
posterior cranial fossa
temporal bone
internal auditory meatus transmits CN7 to ___ (3) and CN8 to ___
stylomastoid foramen
petrotympanic fissure
greater petrosal foramen
membranous labyrinth
stylomastoid foramen contains CN7 ___ fibers
SVE
petrotympanic fissure contains CN7 ___ fibers, aka ___ n.
GVE
SVA
chorda tympani
GVE fibers of chorda tympani nerve synapse in ___ ganglion
submandibular
greater petrosal foramen contains CN7 ___ fibers, aka ___ n.
these fibers terminate at ___ ganglion
GVE
greater petrosal
pterygopalatine
jugular foramen transmits ___ (4) from ___ to ___ through ___
CN9
CN10
CN11
internal jugular vein
posterior cranial fossa
base of skull
temporal and occipital bones
foramen magnum transmits ___ (2) from ___ to ___ through ___
brain stem
spinal part of CN11
posterior cranial fossa
base of skull
occipital bone
cavernous sinus contains ___ (7)
CN3
CN4
CNV1
CNV2
CN6
postgang. sympathetic fibers
internal carotid ar.
CN12 lesion causes ___lateral deviation of ___
ipsi
tongue
CN5 lesion causes ___lateral deviation of ___
ipsi
jaw
CN10 lesion causes ___lateral deviation of ___
contra
uvula
CN11 lesion causes ___lateral rotation of ___
contra
head
CN11 lesion causes ___lateral shoulder droop
ipsi
CN7 UMN lesion causes ___
contralateral lower face palsy
CN7 LMN lesion causes ___
this is aka ___
ipsilateral upper and lower face palsy
Bell's palsy
Bell's palsy is associated with ___ (6)
AIDS
Lyme disease
HZV
sarcoidosis
tumors
DM
K sounds test
CN10
L sounds test
CN12
M sounds test
CN7
all muscles with glossus in their names except ___ are innervated by ___
palatoglossus
CN12
all muscles with palat in their names except ___ are innervated by ___
tensor veli palatini
CN10
palatoglossus is innervated by ___
CN10
tensor veli palatini is innervated by ___
CNV3
___ tone on ___ receptors causes ciliary muscle relaxation for accomodation
ACh
M3
___ tone on ___ receptors causes secretion of aqueous humor
NE
beta adrenergic
___ tone on ___ receptors causes sphincter pupilae contraction
ACh
M3
___ tone on ___ receptors causes pupil dilator contraction (mydriasis)
NE
alpha1 adrenergic
___ glaucoma is insidious
___ glaucoma is acute
open angle
closed angle
angle which distinguishes open and closed angle glaucoma is between ___
and ___
iris
cornea
in open angle glaucoma, flow is obstructed because ___
canal of Schlemm is occluded
in closed angle glaucoma, flow is obstructed because ___
iris is compressing trabecular meshwork
___ glaucoma is an emergency
closed-angle
8 risk factors for cataract
smoking
alcohol
sunlight
galactosemia
galactokinase deficiency
DM
trauma
infection
___ lesion causes superior quadrantanopia
this can be caused by a ___ stroke
part of visual pathway affected is ___
temporal lobe
MCA
Meyer's loop
___ causes inferior quadrantanopia
this can be caused by a ___ stroke
part of visual pathway affected is ___
parietal lesion
MCA
dorsal optic radiation
caloric stimulation with cold water has ___lateral slow phase deflection and
___lateral fast phase deflection
ipsi
contra
caloric stimulation with warm water has ___lateral slow phase deflection and
___lateral fast phase deflection
contra
ipsi
___% of Alzheimer's is familial
2 kinds of familial AD
___ is more common
10
early onset
late onset
late onset
3 genes associated with early onset familial AD
APP
presenilin-1
presenilin-2
APP is on chromosome ___
21
gene associated with late onset familial AD
ApoE4
amyloid plauqes are made of ___
they are intra/extracellular
Abeta
extra
neurofibrillary tangles are made of ___
they are intra/extracellular
hyperphosphorylated tau
intra
degree of dementia correlates better with # of ___ than with # of ___.
NFTs
amyloid plaques
Pick's disease is aka ___
main histopath finding is ___
frontotemporal dementia
Pick bodies
Pick bodies are made of ___
tau
FTD affects anterior/posterior temporal lobe
anterior 1/3
histopath finding in Lewy Body Dementia
these are made of ___
Lewy Body
alpha synuclein
prions in CKD cause ___ structure to change to ___
alpha helix
beta sheet
2 CSF findings in MS
elevated protein
oligoclonal IgG bands
gold standard for MS dx
MRI
T/F: GBS can cause facial paralysis
true
CSF finding in GBS: high ___ with normal ___
protein
cell count
ADEM occurs after ___ (2)
neuropathology is ___
infection
vaccination
demyelination
charcot-marie-tooth is aka
neuropathology of types 1, 3 and 4 is ___
neuropathology of type 2 is ___
hereditary motor and sensory neuropathy
demyelination
axonal
5 kinds of generalized seizure
tonic-clonic
tonic
atonic
myoclonic
absence
top 2 causes of new onset seizures in non-elderly adult
tumor
trauma
___ is always present with peripheral vertigo
nystagmus
nystagmus in peripheral vertigo is always ___
horizontal
nystagmus in central vertigo can be ___ and ___
bidirectional
vertical
hearing loss or tinnitus is primarily associated with ___ vertigo
peripheral
typical duration of migraine
4--72 hr
3 proteins released during migraine
substance P
CGRP
vasoactive peptides
neurocutaneous syndromes are aka ___
4 neurocutaneous syndromes
Sturge-Weber
tuberous sclerosis
neurofibromatosis 1
von Hippel-Lindau
Sturge-Weber has ___ (4)
port-wine stain
ipsilateral leptomeningeal angioma
mental retardation
pheochromocytoma
port-wine stain in Sturge-Weber is located ___ly
in V1 dermatomal distribution
T/F: Sturge-Weber is genetic disorder
false: sporadic
2 histological kinds of growths in tuberous sclerosis
hamartoma
hamartoblastoma
tuberous sclerosis growths affect ___ (3)
CNS
skin
organs (kidneys, heart, lungs)
tuberous sclerosis CNS growths are ___s
hamartoma
facial growths in tuberous sclerosis are called ___ or ___
histologic type of these growths is ___
angiofibroma
sebaceous adenoma
hamartoma
heart tumor in tuberous sclerosis
rhabdomyoma
kidney tumor in tuberous sclerosis
angiomyolipoma
CNS tumor in tuberous sclerosis
subependymal giant cell astrocytoma
cardiac valve abnormality in tuberous sclerosis
mitral regurg
skin patches in tuberous sclerosis are hyper/hypopigmented
patches are called ___
hypo
ash-leaf spots
tuberous sclerosis has shagreen patches, which are ___
leathery skin
tuberous sclerosis is a ___ trait
AD
iris abnormality in neurofibromatosis 1
Lisch nodules
Lisch nodules are pigmented ___s
hamartoma
intracranial tumor in neurofibromatosis 1
optic glioma
abdominal tumor in neurofibromatosis 1
pheochromocytoma
neurofibromatosis 1 is a ___ trait linked to chromosome ___
AD
17
4 kinds of tumor in von Hippel-Lindau
cavernous hemangioma
hemangioblastoma
renal cell carcinoma
pheochromocytoma
von Hippel-Lindau cavernous hemangiomas occur in ___ (3)
skin
mucosa
organs
RCC in von Hippel-Lindau is ___
bilateral
hemanigoblastomas in von Hippel-Lindau occur in ___ (3)
retina
brain stem
cerebellum
von Hippel-Lindau is a ___ trait linked to chromosome ___
AD
3
phakomatoses which cause pheochromocytoma
Sturge-Weber
neurofibromatosis
von Hippel-Lindau
phakomatoses which cause cafe-au-lait spots
neurofibromatosis 1
von Hippel-Lindau
4 kinds of primary brain tumors
glioma
meningioma
neuronal tumors
poorly differentiated
3 kinds of glioma
astrocytoma
oligodendroglioma
ependymoma
3 kinds of astrocytoma
well-differentiated
anaplastic
glioblastoma
top 3 1' intracranial tumors, age over 15 (IDOOF)
glioblastoma/anaplastic astrocytoma
meningioma/nerve sheath
Schwannoma
top 2 intracranial tumors, age <15
well-diff astrocytoma
medulloblastoma (PNET)
___s are 80% of adult 1' brain tumors. they occur most commonly in ___.
astrocytoma
cerebral hemispheres
astrocytomas stain for ___. their malignant potential can be measured with ___ staining, which labels ___.
glial fibrillary acidic protein (GFAP)
Ki67
dividing cells
tumors which take up radiocontrast are more/less malignant
more
4 grades of astrocytoma
pilocytic
fibrillary diffuse
anaplastic
glioblastoma
pilocytic astrocytomas occur most commonly in ___. they are benign/malignant and have ___ fibers.
cerebellum
benign
Rosenthal
fibrillary astrocytoma has high/low Ki67 index
cellularity is high/low and atypia is high/low.
low
high
low
glioblastoma has the features of ___ plus ___ (2)
anaplastic astrocytoma
necrosis
endothelial/vascular proliferation
necrosis in glioblastoma is surrounded by ___
pseudopalisading cells
endothelial proliferation in glioblastoma is caused by ___ produced by tumor
VEGF
pseudopalisading is caused by release of ___ by ___
growth factors
dying cells
2 early mutations in astrocytoma transformation
2 early protein synthesis changes in astrocytoma
17p-
p53
PDGFR overexpression
p14 downregulation
1' glioblastoma happens without ___
preexisting low grade astrocytoma
___ (molecular process) is important in 1' glioblastoma,
___ is important in 2'.
EGFR overexpression
p53 mutation
oligodendrogliomas occur at age ___ and are located mostly in ___
30--50
cerebral hemispheres
4 histopath findings in oligodendroglioma
small round nucleus
perinuclear halo ("fried egg")
anastomosing capillaries ("chicken wire")
calcification
oligodendroglioma has ___ GFAP stain and high/low Ki67 index
negative
low
ependymomas in children occur near ___, in adults in ___.
4th ventricle
SC
ependymoma cells form ___ or perivascular ___.
rosettes
pseudorosettes
ependymoma has ___ GFAP and ___ cytokeratin
positive
positive
___ (2) ependymomas have better prognosis.
prognosis is better/worse in adults than children.
spinal
supratentorial
better
medulloblastoma is more common in children/adults. it occurs in ___ of cerebellum.
children
vermis
medulloblastoma stains positive for ___ (3).
neuron specific enolase
synaptophysin
Ki67
___ rosettes may be present in medulloblastoma. GFAP is usually ___.
Homer-Wright
negative
___ is only 1% of intracranial tumors but is the most common in immunosuppressed
1' CNS lymphoma
___ is present in neoplastic ly cells in 1' CNS ly.
EBV genome
prognosis in 1' CNS ly is good/bad
bad
___ spread is common in 1' CNS ly
periventricular
1' CNS ly is usually ___ ly
DLBCLy
1' CNS ly can be detected with ___ stain
CD20
meningiomas arise from ___ cells and are attached to ___
arachnoid
dura
the ___ variant of meningioma is flat and causes ___
en plaque
hyperostotic rxn
meningiomas are more common in men/women
women
multiple meningiomas are suggestive of ___
neurofibromatosis type 2
most meningiomas are benign/malignant, but tend to ___
benign
recur
most adult 1' brain tumors are ___tentorial
supra
most childhood 1' brain tumors are ___tentorial
infra
____ is a tumor which can have spindle cells with whorled pattern and psammomma bodies
meningioma
___ is associated with bilateral acoustic Schwannomas
neurofibromatosis 2
pituitary adenoma is most commonly a ___
prolactinoma
2 tumors associated with 4th ventricle compression
medulloblastoma
ependymoma
most common childhood supratentorial primary tumor
craniopharyngioma
craniopharyngiomas are derived from
they commonly exhibit ___
rathke's pouch
calcification
hemangioblastomas are most commonly in ___
they are associated with ___
they commonly make ___, which can cause ___
cerebellum
von Hippel-Lindau
EPO
2' polycythemia
2 kinds of cerebral herniations in terms of dural compartments
transfalcine
transtentorial
2 directional kinds of transtentorial herniations
horizontal
vertical
horizontal transtentorial herniation causes ___ (radiological sign)
this is associated with ___
Kernohan's notch
ipsilateral (?) Babinski
2 kinds of vertical transtentorial herniation
central
uncal-parahippocampal
uncal herniation is associated with ipsilateral ___ (2) and contralateral ___
CN3 palsy
hemiparesis
homonymous hemianopia
ipsilateral hemiparesis in uncal herniation is from ___
contralateral Kernohan's notch
(compression of crus cerebri)
contralateral homonymous hemianopia
in uncal herniation is from ___
compression of ipsilateral PCA
caudal displacement of brain stem in uncal herniation can cause ___ hemorrhages
via rupture of ___
Duret
paramedian a.
1 heterogenously enhancing brain lesion
GBM
1 uniformly enhancing brain lesions
meningioma
9 ring-enhancing brain lesions
mets
abscess
glioblastoma
infarct
contusion
AIDS (toxoplasmosis)
1' CNS Ly
demyelination
resolving hematoma
mets are usually ___ enhancing but are sometimes ___ enhancing
ring
uniformly
5 classes of antiglaucoma drugs
alpha agonist
beta blocker
carbonic anhydrase inhibitor
parasympathomimetic
prostaglandin
2 main drugs for glaucoma and their families
timolol (beta blocker)
pilocarpine (parasympathomimetic)
alpha agonists work for glaucoma by ___ing
the mechanism is ___
reducing aqueous humor production
vasoconstriction
___ is an alpha agonist contraindicated in closed angle glaucoma
the reason is ___
epinephrine
mydriasis exacerbates outflow obstruction in trabecular meshwork
___ is an alpha agonist which doesn't cause pupillary change
brimonidine
2 non-selective beta blockers for glaucoma
timolol
carteolol
1 beta1 selective blocker for glaucoma
carteolol
T/F: beta blockers cause pupillary change
false
carbonic anhydrase inhibitor for glaucoma
mechanism is ___
acetazolamide
bicarb ions are required for fluid transport in ciliary body
2 direct PARA-mimetics for glaucoma
pilocarpine
carbachol
2 indirect PARA-mimetics for glaucoma
physiostigmine
echothiophate
PARA-mimetics work in glaucoma by ___ing
this causes ___
inducing miosis
alleviating pressure on canal of Schlemm
prostaglandin for glaucoma
latanoprost
latanoprost is aka ___
it works by ___ing
a side effect is ___
PGF2alpha
increasing aqueous drainage
darkening iris
3 first line drugs for generalized
tonic-clonic (GTC) seizures
these drugs are also good for ___ (2) seizures
phenytoin
carbamazepine
valproic acid
simple partial
complex partial
5 non-first-line drugs for:
GTC,
simple partial, and
complex partial seizures
lamotrigine
gabapentin
topiramate
phenobarbital
levetiracetam
phenytoin mechanism
Na+ channel inactivation
carbamazepine mechanism
Na+ channel inactivation
valproic acid mechanism (2)
Na+ channel inactivation
GABA_A agonism
lamotrigine mechanism
Na+ channel inactivation
gabapentin mechanism
HVA Ca2+ channel inactivation
topiramate mechanism (2)
Na+ channel inactivation
GABA_A agonist
phenobarbital mechanism
GABA_A agonist
2 drugs for simple + complex partial seizures only
tiagabine
vagabatrin
vigabatrin mechanism
GABA_A agonism
vagabatrin GABA_A agonism is via ___
GABA transaminase inhibition
tiagabin mechanism
GABA_A agonism
tiagabin GABA_A agonism is via ___
GABA reuptake inhibition
1st-line drug for absence seizures
ethosuximide
ethosuximide mechanism
thalamic T-type Ca2+ channel block
1st line drug for trigeminal neuralgia
carbamazepine
2 non-seizure indications for gabapentin
peripheral neuropathy
bipolar disorder
phenobarbital is 1st-line drug for ___ (2 populations)
pregnant women
children
in addition to GTC and partial seizures, valproic acid is indicated for ___ (2)
absence
myoclonic
1st line drug for acute status epilepticus
benzodiazepine
2 benzodiazepines for status epilepticus
diazepam
lorazepam
benzodiazepine mechanism
GABA_A agonism
3 AEDs which cause Stevens-Johnson syndrome
carbamazepine
ethosuximide
lamotrigine
3 AEDs which induce CYP450
phenobarbital
phenytoin
carbamazepine
2 AEDs which cause blood disorders
carbamazepine
phenytoin
blood disorder caused by carbamazepine
agranulocytosis
blood disorder caused by phenytoin
megaloblastic anemia
2 AEDs which cause ataxia + diplopia
1 AED which causes only ataxia
carbamazepine
phenytoin
gabapentin
3 AEDs which cause fetal malformations
carbamazepine
phenytoin
valproic acid
3 AEDs which cause endocrine disorders
carbamazepine
phenytoin
valproic acid
endocrine disorder associated with carbamazepine
SIADH
endocrine disorder associated with phenytoin
hirsutism
endocrine disorder associated with valproic acid
weight gain
AED associated with kidney stones + weight loss
topiramate
AED associated with SLE-like syndrome
phenytoin
phenytoin teratogenesis is aka ___
fetal hydantoin syndrome
phenytoin causes ___ anemia by ___ing
megaloblastic
blocking folate absorption
barbiturates increase the ___ of the GABA_A channel
opening duration
___ is an AED associated with hepatotoxicity
carbamazepine
2 AEDs which have additive cardio-respiratory depression with alcohol
barbiturate
benzodiazepine
drugs with ___ blood solubility have rapid induction
low
drugs with ___ lipid solubility have rapid induction
high
MAC stands for ___ and is inversely related to ___
minimum alveolar concentration
potency
MAC is the concentration at which ___
50% of population is anesthetized
MAC is greatest for ___
babies
N2O has ___ blood solubility and ___ lipid solubililty
low
low
induction speed goes with ___
potency goes with ___
blood (in)solubility
lipid solubility
halothane has ___ blood solubility and ___ lipid solubility
high
high
gas tension in lungs depends on ___ (2)
respiratory rate
tidal volume
gas tension in blood depends on ___ aka ___
blood/gas partition coeffcient
solubility
gases with increased ___ require more gas to saturate tissue
AV concentration gradient
inhaled anesthetics cause ___ (2) depression, and cerebral ___ (2)
myocardial
respiratory
increased blood flow
decreased metabolic demand
GI effect of inhaled anesthetics
nausea/emesis
SE of halothane
hepatotoxicity
SE of methoxyflurane
nephrotoxicity
SE of enflurane
convulsions
SE of N2O
expansion of trapped gas
thiopental has ___ lipid solubility
induction is fast/slow
effect is terminated by ___
high
fast
redistribution to tissues
thiopental causes ___ cerebral blood flow
decreased
___ is a benzo used for endoscopy
SEs are ___ (3)
OD is treated wtih ___
midazolam
respiratory depression
amnesia
hypotension
flumazenil
___ is an arylcyclohexylamine
it is a ___ analog
mechanism is ___
ketamine
PCP
NMDA block
ketamine causes ___ cerebral blood flow
increased
propofol is used for ___
it works on ___
rapid induction
GABA_A
3 ester local anesthetics
procaine
cocaine
tetracaine
procaine is aka ___
novocaine
amide local anesthetics have 2 ___s in the name
e.g., ___
i's
lidocaine
all the local anesthetics have ___ in their structure
3' amine
3' amine local anesthetics cross membranes as ___
and bind channel as ___
uncharged (3')
charged
large/small diameter nerves are blocked first
small
myelinated/unmyelinzted nerves are blocked first
myelinated
size/myelination predominates in speed of block
size
sequence of (4) sensations blocked by local anesthetics
pain
temperature
touch
pressure
all local anesthetics except for ___ are given with vasoconstrictor
cocaine
local anesthetic SE
CNS excitation
bupivacaine SE
cardiotoxicity
cocaine SE
arrhythmia
2 kinds of muscle relaxants
depolarizing
nondepolarizing
___ is a depolarizing muscle relaxant
it is broken down by ___ but not ___
succinylcholine
butyrylChE
AChE
butyrulChE is aka ___
pseudoChE
succinylcholine causes ___ (2)
for this reason it is contraindicated in ___
hyperkalemia
hypercalcemia
burn patients
during phase 1 of depolarizing muscle block,
membrane is ___ed
block is ___ed by ChEI
antidote is ___
depolarized
potentiated
doesn't exist
during phase 2 of depolarizing muscle block,
membrane is ___ed
block is ___ed by ChEI
antidote is ___ (2)
(re)polarized
reversed
ChEI
non-depolarizing blocker
nondepolarizing muscle blockers are called ___ or end in ___ or ___
they are competitive/noncompetitive ACh antagonists
tubocurarine
curium
curonium
competitive
competitive muscle block can be reversed by ___ (2)
ChEI
depolarizing muscle blocker
post-tetanic potentiation occurs with ___ (2)
nondepolarizing block
phase 2 depolarizing block
fasciculations occur with ___
depolarizing block
non-depolarizing block affects __ first and ___ last
___ recovers first
eyes
diaphragm
diaphragm
___ is used for malignant hyperthermia
mechanism is ___
dantrolene
prevents release of Ca2+ from SR
PD drug classes
Bromocriptine (DA agonists)
Amantadine (DA secretagogue)
L-Dopa
Selegeline (MAOBIs)
Antimuscarinics
COMTIs
2 non-ergot DA agonists for PD
ropinirole
pramipexole
amantadine SE
ataxia
2 COMTIs
entacapone
tolcapone
PD antimuscarinic
these work on ___ but not ___
benztropine
tremor
bradykinesia
L-dopa SE
arrhythmia
L-dopa is given with ___
this does ___
carbidopa
inhibits dopa decarboxylase
long term use of L-dopa causes ___ after administration
and ___ between doses
dyskinesia
akinesia
2 alzheimer's drugs
memantine
donepezil
memantine mechanism
NMDA blocker
memantine prevents ___
excitotoxicity
donepezil mechanism
AChEI
in huntington's, ___ is high and ___ (2) are low
DA
GABA
ACh
2 amine-depleting drugs for huntington's
reserpine
tetrabenazine
anti-DA drug for huntington's
haloperidol
sumatriptan mechanism
5-HT1B/1D blocker
sumatriptan has short/long t1/2
short (<2h)
2 sumatriptan SEs
coronary vasospasm
tingling
2 common lumbar disc prolapses
L4-5
L5-S1
pain from L4-5 disc prolapse is over ___ joint, ___, and ___ thigh and leg
sacroiliac
hip
lateral
numbness from L4-5 disc prolapse is from ___ leg, and ___
lateral
1st 3 toes
weakness from L4-5 disc prolapse is for ___
on exam this manifests as ___ (2)
foot dorsiflexion
difficulty walking on heels
foot drop
muscles atrophied from L4-5 disc prolapse are ___
reflex anomalies from L4-5 disc prolapse are ___
minimal
minimal
pain from L5-S1 disc prolapse is over ___ joint, ___, and ___ thigh and leg
sacroiliac
hip
posterolateral
numbness from L5-S1 disc prolapse is from ___ leg, and ___
posterior (gastrocnemius)
lateral heel + foot
weakness from L5-S1 disc prolapse is for ___
on exam this manifests as ___
platarflexion
difficulty walking on toes
muscles atrophied from L5-S1 disc prolapse are ___
reflex anomalies from L5-S1 disc prolapse are ___
gastrocnemius, soleus
ankle jerk