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116 Cards in this Set

  • Front
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alpha-agonists

glaucoma drugs & mechanism
epinephrine
brimonidine

v synthesis
beta-blockers

glaucoma drugs & mechanism
timolol
betaxolol
carteolol

v secretion
diuretics

glaucoma drugs & mechanism
acetazolamide

v secretion 2^
v HCO3- 2^
- carbonic anhydrase
epinephrine s/e's
mydriasis
stinging

do not use in closed-angle glaucoma (mydriasis exacerbates closed angle glaucoma)
cholinomimetics for glaucoma: s/e's on the eye
CholinoMimetics

Cyclospasm
Miosis

2^ contraction of ciliary muscle & sphincter
latanoprost s/e
darkens iris
latanoprost is a ...
an anolog of prostaglandin F 2-alpha
latanoprost moa
^ outflow
cholinomimetics

glaucoma drugs & mechanism
direct
--pilocarpine
--carbachol

indirect
--physostigmine
--echothiophate

-- ^ outflow
-- contract ciliary muscle --> open trabecular meshwork
_ is drug for acute angle closure glaucoma
pilocarpine
3 opioid receptors
mu = morphine
delta = enkephalin
kappa = dynorphin
opioid analgesics mechanism
oPen Potassium K+ channels
Close Ca++ channels

--> v synaptic transmission

inhibit release of
substance P and SANG: serotonin, ACh, NE, glutamate
cough suppression
dextromethorphan
opioids for diarrhea
loperamide
diphenoxylate
opioids Rx
pain

--Cough suppression (dextromethorphan)
--Diarrhea (loperamide, diphenoxylate)
--acute pulmonary Edema
opioid analgesics s/e's
"CAMeRA"

constipation
addiction
miosis
respiratory depression
additive CNS depression
treat opioid toxicity with
naloxone
naltrexone

(these are opioid receptor antagonists. aka Narcan)
tolerance does not develop to opioids' ______
miosis
constipation
_ causes less respiratory depression than opioids b/c moa...?
butorphanol

partial agonist at mu

agonist at kappa
butorphanol moa
partial agonist at mu

agonist at kappa
butorphanol s/e
withdrawal if on full agonist
tramadol moa
S^O^N

very weak Opioid agonist

inhibits Serotonin reuptake
inhibits NE reuptake
tramadol Rx
chronic pain
tramadol s/e
similar to opioids

lowers seizure threshold
mlf syndrome aka
internuclear ophthalmoplegia
internuclear ophthalmoplegia--

(5)
--aka MLF (medial longitudinal fasciculus) syndrome

--medial rectus palsy on attempted lateral gaze

--nystagmus in abducting eye

--normal convergence

--MS patients
_ pts have ^ risk of Alzheimer's
Down syndrome
familial alzheimer's genes
Early onset
--APP
--presenilin-1
--presenilin-2

Late onset
--ApoE4
------------------------------

ApoE2 is protective
dementia definition
v
cognitive ability
memory
function

with intact consciousness
alzheimer's findings
cortical atrophy
v ACh
senile plaques
neurofibrillary tangles
senile plaques

vs

neurofibrillary tangles
senile plaques: extracellular beta-amyloid

-->amyloid angiopathy
--> hemorrhage

neurofibrillary tangles: intracellular phosphorylated tau

--> insoluble cytoskeletal tangles

correlate with degree of dementia
beta amyloid synthesis
from cleaving APP (amyloid precursor protein)
pick's disease
DAP PAP

dementia
aphasia
parkinsonism

--personality changes

--atrophy: frontotemporal, except not posterior 2/3 of superior temporal gyrus

--Pick bodies (intracellular aggregated tau)
Lewy body dementia sxs
Houston PD

hallucinations
parkinsonism
dementia
Lewy body dementia cause
alpha-synuclein defect
alpha-synuclein defect causes
Lewy-body dementia
prion protein structural pathophys
alpha helix --> beta-sheet [resistant to proteases]
clinical features of Creutzfeld-Jacob
rapidly progressive (weeks to months)

myoclonus
myoclonus
brief, involuntary twitching
misc. causes of dementia (5)
intellectually, VHS is a WMd

Vitamin B12 deficiency
HIV
Syphilis

Wilson's disease
Multi-infarct (2nd most common cause in elderly)

{d = dementia's misc. causes!}
MS is ____

epidemiology
autoimmune demyelination

relapsing/remitting course

women
20's & 30's
whites
MS sxs
the Holy Hallooing MOB committed a S I I I N

hemiparesis
hemisensory

MLF syndrome
optic neuritis
bladder/bowel

scanning speech
intention tremor
--incontinence
--internuclear ophthalmoplegia
nystagmus
MS rx
--beta-interferon
--immunosuppressants

symptomatic rx for
--neurogenic bladder
--spasticity
--pain
MS dx
M O P =

MRI

oligoclonal bands (IgG) in CSF

periventricular plaques (oligodendrocyte loss; reactive gliosis)
Guillain-Barre is
autoimmune
demyelination

peripheral nerves
motor fibers of central roots (sensory effect is less severe)
Guillain-Barre sxs
symmetric ascending weaknesss

facial paralysis in 50% of cases

autonomic sxs (cardiac, htn, hypotn)
Guillain-Barre prognosis
almost all recover in weeks to months
Guillain-Barre dx
^ CSF protein (--> papilledema)
normal cell count

=albuminocytologic dissociation
GBS is associated with...
Campylobacter jejuni
herpesvirus
vaccination
stress
GBS rx
**respiratory support**
(b/c can affect diaphragm)

plasmapheresis

IV Ig
misc. demyelinating and dysmyelinating diseases
progressive multifocal leukoencephalopathy

acute disseminated (postinfectious) encephalomyelitis

metachromatic leukodystrophy

charcot-marie-tooth disease
PML (5)
demyelination of CNS

JC virus --> destruction of oligodendrocytes

2-4% of AIDS pts

reactivation of latent JC infection

rapid. usu. fatal
acute disseminated encephalomyelitis (4)
PIMP=
postinfectious
inflammation & demyelination
multifocal
perivenular
what can lead to acute disseminated encephalomyelitis?
infections: e.g. measels, chickenpox

vaccinations: e.g. rabies, smallpox
metachromatic leukodystrophy (4)
recessive

lysosomal storage disease

arylsulfatase A deficiency

sulfatide buildup --> impaired production of myelin
Charcot-Marie-Tooth disease aka
HMSN = hereditary motor & sensory neuropathy
Charcot-Marie-Tooth disease clinical presentation (4)
LE muscle atrophy --> inverted bottle

initially affects peroneal nerve
progressive
a seizure is
synchronized, high-frequency firing
partial seizures
--one area of brain

--most commonly originates in mesial temporal lobe

--often preceded by aura

--can secondarily generalize
partial seizures 2 types
simple--consciousness intact

complex--impaired consciousness
generalized seizures start where?
both hemispheres, from beginning of seizure
5 types of generalized seizures
absence
myoclonic
tonic-clonic
tonic
atonic
absence seizures
petit mal
3 Hz
no postictal confusion

blank stare
myoclonic
quick, repetitive jerks
tonic-clonic is aka
grand mal
lateralization:

migraine
tension
cluster
tension is bilateral

the other two are unilateral
migraine aura may include _
visual
sensory
speech
migraine description (5)
your UH degree is N/A if you're going to PPP on campus like that

unilateral
4-72 hours

nausea
+/- aura

pulsating pain
photophobia
phonophobia
migraine is due to
irritation of CN V

release of

substance P
CGRP
vasoactive peptides
migraine rx
propranolol
NSAIDs
sumatriptan for acute
tension headache
bilateral

>30 min steady pain
cluster headache
males much more commonly BURP and HuRL

unilateral
brief headaches
repetitive
periorbital pain

Horner's
Rhinorrhea
ipsilateral Lacrimation

>> common in males
misc causes of headache
hydrocephalus
arteritis
meningitis
neoplasia
vertigo is...
illusion of movement (you or the room)
vertigo types
peripheral
central
adult brain tumors in order from peak incidence
the GM is a SOP

glioblastoma multiforme
meningioma

schwannoma
oligodendroglioma
pituitary adenoma
childhood brain tumors in order from peak incidence
if you want to make a Pile of Medical Appendages, you'll need a He-man or a Crane

pilocytic astrocytoma
medulloblastoma
ependymoma
hemangioblastoma
craniopharyngioma
mass effects of brain tumors include (3)
seizures
dementia
focal lesions
3 general remarks about brain tumors
1^ brain tumors rarely metastasize

mostly:
adult 1^ tumors--supratentorial
child 1^ tumors--infratentorial

--half of adult tumors are metastases (usu. @ gray-white junction)
notable brain tumors that are astrocytomas. stain for _
glioblastoma multiforme

pilocytic astrocytoma

GFAP
glioblastoma multiforme basic description
1-year life expectancy

cerebral hemispheres

"butterfly glioma" (can cross corpus callosum)

astrocytes stain for GFAP
glioblastoma multiforme morphology (2)
"pseudopalisading" pleomorphic cells surrounding

central necrosis & hemorrhage
meningioma basics (3)
@ convexities of hemispheres & parasaggital region

arises from arachnoid cells

resectable
meningioma morphology
spindle cells concentrically in a whorled pattern

psammoma bodies
schwannoma (5)
often localized to CN VIII
--> acoustic schwannoma

resectable

cerebellopontine angle

S-100

bilateral schwannoma is seen in neurofibromatosis type 2
oligodendroglioma (5)
rare
slow-growing
frontal lobes
psammoma bodies are
laminated calcifications
oligodendroglioma morphology (3)
oligodendrocytes "fried egg" cells -- round nuclei, clear cytoplasm, perinuclear halos

"chicken-wire" capillary pattern

often calcified
pituitary adenoma: usu _. a symptom: __. 2 sequelae.
prolactinoma
bitemporal hemianopia

hyper- or hypopituitarism
_ gives rise to anterior pituitary
rathke's pouch
pilocytic astrocytoma (4)
usu in posterior fossa
may be supratentorial
GFAP
benign
pilocytic astrocytoma morphology (2)
Rosenthal fibers -- eosinophilic, corkscrew fibers

cystic + solid
medulloblastoma (4)
--highly Malignant

--cerebellar

--PNET (it's a primitive neuroectodermal tumor)

--can compress 4th ventricle
--> hydrocephalus
medulloblastoma morph (4)
--rosettes or
perivascular rosettes

--solid

--small blue cells

--radiosensitive
ependymoma (3)
most commonly found in 4th ventricle

can cause hydrocephalus

poor prognosis
ependymoma morphology (2)
perivascular pseudorosettes

rod-shaped blepharoplasts near nucleus
hemangioblastoma (3)
usu cerebellar

assoc. with von Hippel-Lindau if found with retinal angiomas

can --> EPO --> polycythemia
hemangioblastoma morph
foamy cells

high vascularity
craniopharyngioma (5)
benign

can --> bitemporal hemianopsia

most common childhood supratentorial tumor

from remnants of Rathke's pouch

Calcification is common (tooth-enamel like)
4 types of herniation syndromes
cingulate (subfalcine) -- under falx cerebri

transtentorial

uncal

cerebellar tonsillar into foramen magnum
_ herniation can compress _ artery
cingulate (subfalcine)

anterior cerebral artery
peripheral vertigo (3)
more common

inner ear etiology
--semicircular canal debris
--vestibular nerve infection
--Meniere's

delayed horizontal nystagmus
central vertigo (2)
brain stem or cerebellar lesion
--vestibular nuclei
--posterior fossa

immediate nystagmus in any direction. may change directions.
Sturge-Weber
it's fun to Play Inside PVC
My GoSH!

pheochromocytomas
ipsilateral leptomeningeal angiomas

port-wine stains
V1 distribution
congenital, sporadic

can -->
mental retardation
glaucoma
seizures
hemiparesis
tuberous sclerosis
SS SSclerosis is HA RRR D

subependymal giant cell astrocytoma
seizures

shagreen patch
sebaceous adenoma

hamartomas (CNS, skin, organs)
"ash leaf spots"
cardiac Rhabdomyoma
renal angiomyolipoma
retardation
dominant
neurofibromatosis type I is aka
von Recklinghausen's
port-wine stains aka
nevus flammeus
neurofibromatosis type I
P
CLOwN
N
D

Cafe-au-lait spots

Lisch nodules (pigmented iris hamartomas)
Optic gliomas

neurofibromas

pheochromocytomas
NF-1 gene (17)
dominant
von Hippel-Lindau disease
BCD, HPV

--bilateral renal cell carcinoma
--cavernous hemangiomas (skin, mucosa, organs)
--dominant

--hemangioblastoma
(retina, brain stem, cerebellum)
--pheochromocytomas
--VHL (tumor suppressor) (3)
uncal herniation signs (4)
pupil dilation/proptosis -- 2^ stretching CN III

contralateral homonymous hemianopia -- 2^ compression of ipsilateral posterior cerebral artery

ipsilateral paresis 2^ compression of contralateral crus cerebri

Duret hemorrhages --paramedian artery rupture
what artery supplies occipital cortex?
posterior cerebral
uncal herniation: compression of contralateral crus cerebri is aka
Kernohan's notch
metastases are *usually* _ enhancing
ring-enhancing
ring-enhancing lesions
metastases
abscesses
toxoplasmosis
AIDS lymphoma
uniformly-enhancing lesions
lymphoma
meningioma
metastases (usu ring-enhancing)
heterogeneously-enhancing lesion
glioblastoma multiforme