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298 Cards in this Set

  • Front
  • Back
Parkinson's Disease -
What is it
ACh and dopamine must be
in balance for normal,
balanced movement
dec. levels of dopamine
in substantia nigra
idiopathic hypokinetic
When does it start
usu. starts ~50-60 y/o
Life expectancy
life expectancy ~ 9 yrs.
Parkinson's Disease -
Most cases are idiopathic
Insults that lead to
"parkinsonism"
insults dec. dopamine -
postencephalitic
toxic insults -
(carbon disulfide
manganese
MPTP)
others
bihemispheric ischemic
traumatic
iatrogenic (neuroleptic meds)
Parkinson's Disease -
History/PE
Tremor at rest (pill rolling)
PD History/PE
cogwheel rigidity
PD History/PE
bradykinesia
PD History/PE gait
festinating(Sinirlilikten gelen hızlı yürüme eğilimi) gait
PD History/PE posture
stooped posture
PD History/PE posture
unstable posture
PD History/PE face
masked facies
PD History/PE memory ?
memory loss
PD History/PE writing
micrographia
PD History/PE
shy-dragger-
any autonomic dysfunction
Parkinson's Disease -
Tx 1st -
is it from a secondary cause
that can be reversed?
Parkinson's Disease -
Tx then -
2nd question
how does pt. function daily?
tremor but functioning -
> 60 y/o
tremor but functioning -
> 60 y/o - amantidine
tremor but functioning -

< 60 y/o -
tremor but functioning -

< 60 y/o - anticholinergic
PD tx if can't function -
l-dopa-carbidopa
most effective
but most side effects
l-dopa-carbidopa most side effects
"response fluctuations"
Tx fluctuations -
COMT or selegiline
list of meds -
L-dopa/carbidopa - mainstay
bromocriptine
selegiline
entacapone (COMT inhib)
amantadine & anticholinerg -
limited efficacy
If meds fail & dis. advanced-
deep brain stimulation of
GPi and subthal nucleus,
or pallidotomy -
ablation of GPi
(posteroventral GP)
rarely done now
Huntington's -
Hyperkinetic
Huntington's - genetics
AD
Huntington's - brain part
atrophy of caudate
Huntington's - biochemistry
lose GABA
Huntington's - genetics
CAG triple repeats on C4p
anticipation -
prog. expansion
> 39 repeats - mutant genes
Huntington's -
History/PE
Presents ~30-50 y/o
gradual onset of -
chorea
dementia
altered behavior
depression
Huntington's -
Dx
Clinical
CT
MRI
molecular genetic testing
Huntington's -
Tx
No cure
disease cannot be halted
genetic counseling
Huntington's -
Tx - psychosis
haloperidol
Huntington's -
Tx minimize unwanted movements
reserpine -
MCC of dementia in elderly
Alzheimer's -
Alzheimer's -
What is it • senile plaques
- B amyloid
Alzheimer's - • neurofibrillary tangles -
abnorm phosphorylated tau protein
Alzheimer's - • loss of ACh in cortex -
basal nucleus of Meynert
Alzheimer's - • amyloid angiopathy
=> lg lobar hemorrhage
Alzheimer's - brain localisation
• hippocampus affected early
Alzheimer's -
Risk factors - most important
Age
Alzheimer's -
Risk factors syndrome
family history
Down's (> 35 y/o)
Alzheimer's -
Risk factors
female gender
Alzheimer's -
Risk factors chromosomes
21, 14
Alzheimer's -
Risk factors chromosome 1 -
younger age
Alzheimer's -
Risk factors chromosome 19
- older
Alzheimer's -
Risk factors genetics of high rate of Alzheimer's
homozygous for ApoE4 -
Alzheimer's -
????usually 1st sign
then ?????deficits
Amnesia usually 1st sign
then language deficits
Alzheimer's -
History/PE
Amnesia usually 1st sign
then language deficits
acalculia
depression
agitation
apraxia
Alzheimer's -
Evaluation Dx
Dx of exclusion
def. Dx only on autopsy
Alzheimer's -
Evaluation MRI or CT -
diffuse cortical
and subcortical atrophy
Alzheimer's -
Evaluation Neuropsych testing -
distinguish between
dementia and depression
Alzheimer's -
Tx mentality
Supportive therapy
Alzheimer's -
Tx first-line therapy
Cholinesterase inhibitors -
Cholinesterase inhibitors -
donepezil
rivastigmine
galantamine
Alzheimer's - may slow cognitive decline
Vit E (a-tocopherol) -
Alzheimer's -
Complications
death usually secondary to
aspiration pneumonia or
other infections
Alzheimer's - death
Survival is 5-10 yrs from
onset of sxs
Delirium -
What is it
impairment of consciousness -
dec. awareness of your envi
can't maintain attention
Delirium -
What is it caused by
Caused by acute illness,
infection or drug toxicity
Delirium -
Timing of onset
Sudden onset
Delirium -

Course
Reversible (usually)
Dementia -
What is it caused by
Timing of onset
Course
Caused by anatomic changes
in the brain
Slow, gradual onset
Irreversible
Subarachnoid Hemorrhage -
What is it
MCC
Due to bleeding
from ruptured aneurysm
MCC - head trauma
(Circle of Willis)
(considered separate d/o)
spontan - ruptured aneurysm
Subarachnoid Hemorrhage -
spontan -
(Circle of Willis)
(considered separate d/o)
ruptured aneurysm
usually congenital berry
associated with APKD,
coarctation of aorta
Subarachnoid Hemorrhage -
other cause
- AV malformation
Subarachnoid Hemorrhage -
age of onset
~50-60 y/o
Subarachnoid Hemorrhage -
mortality
high mortality
Subarachnoid Hemorrhage -
History/PE onset
Sudden-onset headache
Subarachnoid Hemorrhage -
History/PEjeneric sentences
"worst headache of my life"
Subarachnoid Hemorrhage -
History/PE
loss of consciousness
fever
n/v
neck stiffness
seizure
Subarachnoid Hemorrhage -
History/PE CN3 palsy -
if berry aneurysm
may be preceded by
milder sentinel headaches
weeks earlier
Subarachnoid Hemorrhage -
Dx
CT without contrast immed.
Subarachnoid Hemorrhage -
Dx CT
blood appears white
Subarachnoid Hemorrhage -
Dx if CT neg -
LP immediately
ck for xanthochromia
Subarachnoid Hemorrhage -
Dx no LP if...... why
inc. ICP -
sudden dec. in CSF pressure
can cause further bleeding
Subarachnoid Hemorrhage -
Dx to pinpoint location
4-vessel angiography
Subarachnoid Hemorrhage -
Tx to Prevent 2nd rupture -
Prevent 2nd rupture -
most likely in 1st 48 hrs
obliterate aneurysm
Subarachnoid Hemorrhage -
Tx
IV fluids
keep BP OK
Subarachnoid Hemorrhage -
Tx to prevent vasospasm
nimodipine
Subarachnoid Hemorrhage -
Tx to prevent seizure
phenytoin
Subarachnoid Hemorrhage -
Tx to lower ICP -
raise head of bed,
hyperventilation
Subarachnoid Hemorrhage -
Tx surgery -
clip aneurysm
IR (stent-assisted) coiling
Subarachnoid Hemorrhage -
Tx pain meds -
no NSAIDs
Subarachnoid Hemorrhage -
Complications 2nd rupture -
esp. with aneurysm
Subarachnoid Hemorrhage -
Complications extend into brain parenchyma-
esp. with AVM
Subarachnoid Hemorrhage -
Complications others
arterial vasospasm
obstructive hydrocephalus
Epidural Hematoma -
Often due to???? trauma
usually ??????? fracture
tear of ????????????Art.
Often due to blunt trauma
usually lateral skull fracture
tear of Middle Meningeal Art.
Epidural Hematoma -
History/PE Lucid interval
- min. to hrs.
then headache
progressive obtundation
hemiparesis
"blown pupil"
"blown pupil"
A mydriatic pupil will remain excessively large even in a bright environment and is sometimes colloquially referred to as a "blown pupil"
Epidural Hematoma -
Dx
CT -
Epidural Hematoma - CT -
????shaped hyperdensity
lens-shaped
convex hyperdensity
close observation and
serial neuro exams
before surgery
Epidural Hematoma -
Tx
Neurosurgical evacuation
Subdural Hematoma -
What is it
Usually after head trauma
rupture of bridging veins
cortex to dural sinuses
esp. elderly & alcoholics
Subdural Hematoma -
History/PE
Headache
change in mental status -
Subdural Hematoma -
days to weeks
can present as dementia
in elderly
contralateral hemiparesis
may have remote h/o fall
Subdural Hematoma -
Dx
CT -
CT -
crescent-shaped
concave hyperdensity
Subdural Hematoma -
Tx
Neurosurgical evacuation
blood may regress spontan-
eously if chronic
corticosteroids
phenytoin
Parenchymal Hemorrhage -
Causes
HTN (usually in basal ganglia)
tumor
Parenchymal Hemorrhage -
Causes - elderly
amyloid angiopathy
Parenchymal Hemorrhage -
Causes vascular malformations -
AVM
cavernous hemangiomas
Parenchymal Hemorrhage -
History/PE
lethargy
headache
focal mtr & sensory deficits
some obtundation
Parenchymal Hemorrhage -
Dx
CT without contrast
check for mass effect
or edema
Parenchymal Hemorrhage -
Tx
Raise head of bed
antiseizure prophylaxis
neurosurgical evacuation -
if mass effect
esp. in posterior fossa
Coma -
What is Rule of 4
1. Thiamine, D50, naloxone
coma cocktail
Coma -
What is Rule of 4
2. 2 mechanisms
bilateral hemisphere or
RAS
Coma -
What is Rule of 4
3. 3 general dis. processes
structural
metabolism
seizures
Coma -
What is Rule of 4
4. 4 key aspects to exam
Coma -
General Processes: Structural
Hematoma
Infarction
Abscess
Tumor
Abnormal imaging lesion
that occupies space
Coma -
General Processes: Metabolism
Electrolyte, endocrine or
metabolic functions
substrate deprivation -
O2, glucose
vitamin deficiency
organ failure - kidney
toxins -
meds
etoh
drugs
infections
inflammatory dis.
Normal imaging
Coma -
General Processes: Seizures
Status epilepticus
postictal
Coma -
4 aspects of exam
Pupils
eye movement
motor response
ventilation pattern -
acid-base status
Coma - Stabilize the patient -
Tx
Airway
Breathing
Circulation
Coma -
Tx
Reverse the reversible -
coma cocktail
O2
ID and tx underlying cause
Prevent further damage
Broca's Aphasia -
What is it
What part of brain affected
D/o of language production
motor
broken speech
comprehension is intact
expressive or
nonfluent aphasia
post. inferior frontal gyrus
Broca's Aphasia -
Features
Repetition is impaired
Broca's Aphasia - why frustration -
cuz aware
Broca's Aphasia associated with -
arm and face hemiparesis
hemisensory loss
apraxis of oral muscles
Broca's Aphasia often secondary to
left superior MCA stroke
Broca's Aphasia -
Tx
Speech therapy
tx underlying condition
wide range of outcomes
intermediate prognosis
Wernicke's Aphasia -
What is it
D/o of language comprehension
nonsensical production
Wernicke's is wordy
left post. superior temporal
receptive or fluent aphasia
Wernicke's Aphasia -
Features
Neologisms
word substitutions
unaware - no comprehension
secondary to
left inf./post MCA stroke
Wernicke's Aphasia -
Tx
Speech therapy
tx underlying condition
poorer prognosis than Broca's
Brain Neoplasms -
Mets vs. Primary
Benign usually > 65 y/o
Brain Neoplasms -
Mets Metas -
Lots of Bad Stuff Kills Glia
Metas -
Lots of Bad Stuff Kills Glia
Lung Breast Skin Kidney GI
Brain Neoplasms -
Mets ?? Primary
metas > primary
supratentorial
at junction of gray and
white matter
Primary (1o) -MC primary in adults -
glioblastoma and meningioma
most 1o are supratentorial
MC primary in kids -
medulloblastoma & astrocytoma
most 1o are infratentorial
Brain Neoplas ms -
Dx CT with????
CT with contrast
Brain Neoplas ms -
Dx MRI with
gadolinium
Brain Neoplas ms -
Dx CT-guided
Bx
Brain Neoplas ms -
Dx
Bx during surgical tumor
debulking
Brain Neoplasms -
General Principles of Tx
Resection (if possible)
radiation
chemo
palliative tx
corticosteroids -
reduce vasogenic edema
type of therapy depends on -
type of tumor
histology
progression
site
Brain Neoplasms:
Glioblastoma -
Characteristics and
Presentation
Grade IV astrocytoma
MC primary brain tumor
prognosis grave
< 1 year to live
can cross corpus callosum
progresses fast
headache
ICP
Brain Neoplasms:
Glioblastoma -
Tx
Surgical resection
radiation and chemo
have variable results
2nd MC primary
Meningioma -
Meningioma -Characteristics and
Presentation
often incites osteoblastic
reaction in overlying
cranial bones
incidence inc. with age
Meningioma - orig from
dura or arachnoid
Meningioma -prognosis
good prognosis
Brain Neoplasms:
Meningioma -
Tx
Surgical resection
radiation for unresectable
Brain Neoplasms:
Acoustic Neuroma (Cihannoma)
Derived from cihan cells
bilat cihannoma in NF2
Acoustic Neuroma (Cihannoma)Characteristics and
Presentation
Ipsilateral hearing loss
tinnitus
vertigo
signs of cerebellar dysfunction
facial weakness
facial sensory loss
Acoustic Neuroma (Cihannoma)
Surgical removal
Brain Neoplasms:
Astrocytoma -Sibelcanoma
Characteristics and
Presentation
Grades 1 - pilocytic,
mainly kids
grade 2 - diffuse
grade 3 - anaplastic
grade 4 - glioblastoma multif
Sibelcanoma
Characteristics and
Presentation
headache
inc. ICP
can cause unilat paralysis in
CN 5-7 & CN10
Sibelcanoma Tx
Resection if possible
radiation
Brain Neoplasms:
Medulloblastoma - sedanoma
locations
arises from cerebellum
and 4th ventricle
can compress 4th ventricle
may seed subarachnoid space
inc. ICP
sedanoma headache time
morning headaches
sedanoma malignancy
Highly malignant
sedanoma tx
Surgical resection
coupled with
radiation and chemo
Brain Neoplasms:
Ependymoma -zaranoma
Characteristics and
Presentation
Common in kids
arises from ventricles
and spinal cord
commonly found in 4th ventricle
can cause hydrocephalus
-zaranoma
Surgical resection
radiation
Neurofibromatoses -
What are they
NF1 - HOUSE MD
von Recklinghausen
AD
chromosome 17

NF2
chromosome 22
HOUSE MD
2 or more of signs
HOUSE MD skin findingds
neurofibromas (2)
HOUSE MD skin findingds
cafe-au-lait spots (6)
HOUSE MD axillary or inguinal
freckling -
axillary or inguinal
HOUSE MD eye findings
optic glioma
HOUSE MD eye findings
lisch nodules (2)
HOUSE MD eye findings
osseous abnorm
1st degree relative with NF1
NF2 - Dr Coddy
bilat acoustic neuromas
Dr Coddy or
1st deg. relative with NF2
and unilat acoustic neuroma
Dr Coddy or
1st deg. relative with NF2
and neurofibroma,
meningioma,
glioma
Dr Coddy or
schwannoma
HOuse md dx
MRI -
brain
brain stem
spine
derm exam
ophthal exam
family Hx
hearing test
HOuse md
No cure
tx symptoms
surgical removal for
acoustic neuromas
Tuberous Sclerosis - Kucuk zenci eleman neurologic
Seizures - start as infant
mental retardation
Kucuk zenci eleman
skin and eye lesions
Kucuk zenci eleman
small benign tumors -
brain
face
eyes
kidney
other organs
very variable clinical course
Kucuk zenci eleman
AD
chromosome 9
Kucuk zenci velet as an infant
Hx/PE
Infantile spasms
Kucuk zenci velet skin
ashleaf lesions -
hypopigmentation
trunk and extremities
Kucuk zenci velet saCRUM
shagreen patch - lumbosacral
Kucuk zenci velet - nose, cheeks
sebac. adenoma
Kucuk zenci velet tumors
mulberry tumors
Kucuk zenci velet tumors
phakomas
phakomas
benign growths seen as white patches on the retina
mulberry tumors
Nodular astrocytoma of the retina on or about the optic nerve head.
Kucuk zenci velet dX CT -
calcified tubers
periventricular areas
can => astrocytomas (rare)
Kucuk zenci velet Wood's UV lamp -
skin lesions
Kucuk zenci velet DX
EKG
renal US
Kucuk zenci velet TX FOR SEIZURE
Levent kirca or Araklamaci gazeteci
Kucuk zenci velet TX
inc. ICP -
may indicate
a tuber obstructing
Foramen of Murro
surgery
Kucuk zenci velet TX
EKG
LEVENT KIRCA
Clonazepam
Araklamaci gazeteci
valproic acid
Von Hippel-Lindau -
genetics
Dominant teyze
deletion of VHL gene on ch CIRA
Von Hippel-Lindau - hemangioblastoma -
cerebellum
medulla
Von Hippel-Lindau - Kidney
retinal angioma
RCC
pheochromocytoma
Von Hippel-Lindau -
Hx/PE
Headache
N/V
cerebellar Sxs
Von Hippel-Lindau -
Hx/PE
retinal angiomas -
retinal angiomas - place
complication
usu. periphery
can => retinal detachment
Von Hippel-Lindau -
Dx
CT - head, abdo
MRI -
post. fossa emphasis
serpentine signal voids
angiography - vascularity
CBC - polycythemia
VMA levels in urine
ophthal US
Von Hippel-Lindau -
Tx
Surgical resection
or
radiation
Osler-Weber-Rendu BArbara-genetics
AD
BARBARA -also called -
Hereditary Hemorrhagic
Telangiectasia (HHT)
BARBARA telangiectasia and AVM
in
lungs, GI, brain
recurrent epistaxis
BARBARA Hx/PE
Recurrent epistaxis
painless bleeding in bowel
BARBARA hepatic AV fistula -
(hepatomegaly
RUQ pain
pulsatile mass
palpable thrill
audible bruit
high-output CHF
liver failure)
BARBARA hep. enceph -
portosys shunt
neuro complications
BARBARA rt-to-left shunt -
(cyanosis
clubbing
hypoxemia
2ndary polycythemia
exertional dyspnea)
BARBARA tx
Iron
folate
symptomatic tx of epistaxis
embolization,
surgical excision
or ligation of AV fistulas
BARBARA???- contraindicated
ASA
Closed-Angle Glaucoma -
Hasan amca
Med emergency
usu older pts. and Asians
Hasan amca mechanism
iris root plugs opening of
trabecular meshwork
acutely
Hasan amca causes
pupillary dilation
anterior uveitis
dislocation of lens
Hasan amca Hx/PE
Intraocular pressure inc.
very fast
extreme periocular pain
acute red eye
blurred vision
Hasan amca Dx Best diagnostic test -
tonometry
Hasan amca Tx
acetazolamide
pilocarpine - when P drops
Hasan amca - curative
laser iridotomy
Most common form
Glaucoma -
Open-Angle Glaucoma mustesar kemal
Open-Angle Glaucoma bi unilateral??
almost always bilateral
mustesar kemal risk factors -
> 40 y/o
Black
diabetic
myopic
family Hx
diseased trabecular meshwork
obstructs proper drainage
mustesar kemal cause of vision lose
=> intraoc P inc. gradually
progressive vision loss
mustesar kemal vision loss -
moves periph to central
mustesar kemal at end
=> blindness
mustesar kemal
Hx/PE
Asymp initially
mustesar kemal suspect if pt. -
> 35 y/o
freq. lens changes
mild headaches
vision disturbances
impaired adaptation to dark
mustesar kemal earliest defect -
periph nasal fields
cupping of optic disk
mustesar kemal dx
Tonometry
ophthalmic exam of optic n.
central field testing
eval on long-term basis
can be hard to Dx until
advanced stages
Mustesar Kemal tx Prevention
> 40 y/o - exam every 3-5 yrs
inc. risk factor - annually
Mustesar Kemal tx
timolol, betaxolol
pilocarpine
acetazolamide
Mustesar Kemal tx
laser trabeculoplasty -
if meds fail
MCC of permanent bilat
vision loss in elderly
Macular Degeneration -
What is it
Macular Degeneration -
What is it vision loss -
central do not lose periph
Macular Degeneration -
difference between atrophic and exudative form
atrophic - gradual loss
exudative -
faster
damage more severe
Macular Degeneration -
Hx/PE
painless loss of
central vision
Macular Degeneration -atrophic -
irreg pigmentation of
macular region
Macular Degeneration -exudative -
hyperpigmentation
pimple-like elevation of
macula - from hemorrhage
Macular Degeneration -Laser photocoagulation -
may delay loss of central
vision in exudative
Retinal Artery Occlusion -
What is it
From emboli or thrombi
sudden
painless
unilat blindness
Retinal Artery Occlusion -pupil
pupil accommodates but reacts
sluggishly to direct light
Retinal Artery Occlusion - retina
cherry-red spot on fovea
artery may look bloodless
retinal edema
Retinal Artery Occlusion -?????within
8 hrs of onset of Sx
Thrombolysis within
8 hrs of onset of Sx
Retinal Artery Occlusion -dec. intraoc P -
drain ant. chamber
Retinal Artery Occlusion -
IV acetazolamide
Retinal Vein Occlusion - eye exam
Sudden
painless
retinal hemorrhages
cotton wool spots
edema of fundus
elderly
Retinal Vein Occlusion -MCC
- HTN
can => macular dis., glaucoma
Retinal Vein Occlusion -Tx
Laser photocoagulation
Inc. ICP -
Causes Blood -
EDH, SDH, SAH, ICH
spontaneous or traumatic
Inc. ICP -
Causes due to CSF -
hydrocephalus
idiopathic intracranial HTN
Inc. ICP -
Causes due to brain mass -
tumor
Inc. ICP -
Causes due to trauma -
cerebral contusions
Inc. ICP -
Causes due to edema -
trauma
tumors
Inc. ICP -Signs in approx. order
of appearance
N/V and headache
altered mental status
Inc. ICP -Signs in approx. order
of appearance than
in kids - bulging fontanelles
Inc. ICP -Signs in approx. order
of appearance than
papilledema
Inc. ICP -Signs in approx. order
of appearance than
CN palsies - esp. CN6
Inc. ICP -Signs in approx. order
of appearance than
Cushing's Triad -
(HTN
brady
irreg breathing)
Inc. ICP -Signs in approx. order
of appearance than
endstage -
cerebral herniation
Inc. ICP -
Tx -
in order
Make sure BP and resp. good
Inc. ICP -
Tx -
in order
sedation
Inc. ICP -
Tx -
in order
elevate head of bed
Inc. ICP -
Tx -
in order
IV mannitol
Inc. ICP -
Tx -
in order
hyperventilate to CO2 30-35
Inc. ICP -
Tx -
in order
ventriculostomy
Inc. ICP -
Tx -
in order
surgery -
removal of hematoma
decompressive craniectomy
Herniation -
What is it
Types
Dx
Endpoint of untreated masses
or inc. ICP
specific signs and Sxs
depends on type of hernia
and mass lesion
uncal herniation -
CN3 compression:
ipsilat dilated pupil
midbrain compression:
ipsilat hemiplegia
tonsillar herniation -
resp. compromise
Dx -
CT without contrast -
r/o mass lesion or hemorrhage
Guillain-Barre - La Ispanyol
What is it
Acute
rapidly progressive
acq. demyelinating autoimmune
Ispanyol
d/o of periph nerves
Ispanyol
recent C. jejuni infection
viral infection
recent vaccination
Ispanyol process and involvement
Rapidly progressive
ascending paralysis
involves trunk, diaph and CN
autonomic Sxs
areflexia
Ispanyol dx Diffuse demyelination on -
EMG & nerve conduction studies
Ispanyol csf
albuminocytologic dissociation
CSF prot. > 55 mg/dL
Ispanyol tx
ICU -
risk of respiratory failure
plasmapheresis or IVIG
aggressive rehab
MS -
What is it
Acq. demyelinating dis.
may have T cell-mediated
autoimmune pathogenesis
environmental and genetic
MS female-to-male
2:1
MS age geography
20-40 y/o
inc. prev. with gtr distance
from equator
MS risk -
related to where lived
the 1st 15 yrs. of life
MS subtypes -
benign
relapsing/remitting
2o progressive
chronic progressive
MS -
Hx/PE
Mult. neuro complaints
MS -
Hx/PE
sep. in time and space
can't be explained by a
single lesion
MS -
Hx/PE
limb weakness
MS -
Hx/PE
optic neuritis
paresthesias
diplopia
internuclear ophthalmoplegia
MS -
Hx/PE
urinary retention
MS -
Hx/PE
vertigo
MS -
Hx/PE
Sxs wax & wane or progress
MS -
Hx/PE exacerbations -
stress
infections
heat
trauma
vigorous activity
MS -
Dx describe MRI finding
Multiple, asymmetric periven-
tricular lesions in white mtr
MS -
Dx corpus callosum lesions -
pathognomonic
MS -
Dx active lesions enhance with
Gado on MRI
MS -
Dx CSF
inc. CSF IgG
oligoclonal bands
MS -
Tx Acute -
steroids
MS -
Tx treat Sxs - spasticity:
baclofen or zanaflex
MS -
Tx treat Sxs - pain:
phenytoin
MS -
Tx treat Sxs - fatigue:
amantadine or provigil
MS -
Tx treat Sxs -
depression
avoid hot climates
MS -
Tx prophylaxis:
immunomodulators
MS -immunomodulators
reduce no. of attacks, disability
MS Avonex -
once wkly IM
MS Betaseron
- every other day subq
MS Copaxone
- daily subq