PNS Flashcards

1
Q

ALS

A

upper and lower MN signs
degeneration of anterior horn cell
MOTOR ONLY no sensory loss
*fatal: affect swallowing, resp mm

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2
Q

As ALS progresses,

A

weakness, facial/respiratory, paresis–>plegia
NO SENSORY LOSS, NO COG FUNCTION LOSS

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3
Q

HOW DOES ALS usually present?

A
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4
Q

pseudobulbar palsy

A

laugh or cry inappropriately
disconnect btwn emotions and expression
COMMON IN ALS**, MS, strokes

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5
Q

LMN signs in ALS

A

weakness, atrophy, fasciculations
brainstem: jaw, face, palate, tongue, larynx
cervical: neck, arm, hand first
thoracic: diaphragm, back, abdomen
lumbosacral: back, abdomen, leg, foot

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6
Q

how does pain manifest in ALS?

A

cramps, contractures, pressure sores due to lack of mobility

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7
Q

West Nile Virus

A

asymmetric flaccid weakness and hypoactive/absent reflexes
*pure motor

anterior horn cell!!! changes in MRI, B&B affected too!
meningoencephalities
aseptic meningitis

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8
Q

plexopathy presents as

A

very painful at shoulder or hip, weakness in limb, more than one nerve/root distribution

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9
Q

plexopathy is due to

A

trauma
tumor
thoracic outlet syndrome (extra cervical rib)
*diabetes can cause ischemia to plexus (lumbosacral plexus)

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10
Q

mononeuropathy multiplex

A

neuropathy in several different nerves quickly in short period of time

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11
Q

polyneuropathy is

A

length dependent
(feet, then hands when knees get affected, abdomen affected in front)
*stocking/glove distribution

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12
Q

meralgia parasthetica

A

lateral femoral cutaneous nerve (compressed at inguinal ligament), sensory ONLY
***numbness
-Britney Spears
-L2, L3

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13
Q

demyelinating neuropathy

A

weakness without atrophy!
patchy/asymmetric
can be length independent

get better!

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14
Q

causes of demyelinating neuropathy

A
  1. compression/stretch (carpal tunnel, trauma)
  2. GBS and CIDP: inflammatory, get better
  3. multifocal motor neuropathy
  4. diphtheria
  5. Charcot Marie Tooth: gene absent
  6. hereditary neuropathy
  7. MAG neuropathy
  8. leukodystrophies
  9. diabetes
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15
Q

axonal neuropathy

A

most common: diabetes
alcohol (2nd most common)
toxic: vincristine, acrylamide, arsenic
cancer
amyloid
AMAN, AMSAN (axonal GBS)
uremia
collagen vascular diseases

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16
Q

small fiber neuropathy

A

a lot of times is diabetes
pain and temp loss, neuropathic burning pain
discolored skin, less sweat, loss of hair

PAIN, TEMP, AUTONOMIC
not proprioception, not motor
allodynia
emg may be normal!

17
Q

large fiber neuropathy

A

sensory (proprioception) and motor nerves
*numb, walking on foam

18
Q

autonomic neuropathy

A

Orthostatic hypotension
* Arrhythmias
* Severe constipation, urinary retention, erectile dysfunction
* Abnormal sweating
* Early satiety, lightheadedness with meals

19
Q

inflammatory demyelinating polyneuropathies

A

disorders that cause weakness, sensory loss, areflexia
AIDP or GBS are rapid
CIDP are slow

20
Q

AIDP

A

acute inflamm demyelin polyneuropathy
1. tingling/parasthesias
2. severe radicular back pain
3. weakness legs to arms

21
Q

GBS

A

demyelinating

monitor/treat respiratory failure, autonomic dysfunction
rehab early! get better

22
Q

chronic inflammatory demyelinating polyneuropathy

A

mainly motor over sensory
large fiber!
not atrophy (demyelinating)
but areflexic

symmetric weakness of prox and distal

23
Q

diabetic neuropathy does not cause weakness!!! It is probably

A

CIDP in diabetic patient

24
Q

diabetic neuropathies

A

stocking-glove sensory loss
autonomic changes after sensory
does not cause weakness
*can treat PAIN not weakness
neuropathic pain meds can cause sleepiness and dry mouth

25
what is charcot marie tooth disease
distal weakness, atrophy length dependent sensory loss foot deformities (hammer toes) absent reflexes/decreased CHRONIC, slowly prog hereditary!
26
myasthenia gravis
post synaptic autoimmune disorder *with very brief rest, much better! FATIGABLE! EYE MUSCLES! asymmetric ptosis, diplopia -difficulty chewing, dysarthria, dysphagia, nasal speech -hoarse -head drop -limb weakness
27
presynaptic disorder
lambert eaton botulism
28
triggers for MG exacerbation
Emotional upset * Viral illnesses and other systemic illness, fever* Heat * Hypo or hyperthyroidism * Surgery * Menstrual cycle -MEDS
29
ocular cooling for myasthenia gravis
cold makes better conduction across neuromuscular junction antibodies attack ACh junction...
30
what are negative signs of myopathy?
* Weakness * Fatigue * Atrophy * Exercise Intolerance
31
what are positive signs of myopathy?
-Myalgia * Cramps * Contractures * Hypertrophy* Stiffness * Myoglobinuria
32
difference between prox/distal for neuropathy vs. myopathy
myopathy: PROXIMAL WEAKNESS neuropathy: distal
33
what does a myopathy physical exam look like
gower's maneuver (all fours) getting up from chair, reaching high is HARD due to prox weakness ****sensation usually intact DTRs normal/slightly reduced
34
inclusion body myositis
most freq myopathy in patients over 50 yrs prox leg and distal arms (finger flexors, quads) -asymmetric -dysphagia -muscle atrophy
35
myotonic dystrophy type I
most common ADULT myopathy frontal temporal balding can't smell myotonia: sustained contracture of muscles (shake hand, can't release it) eyelid myotonia cardiac problems cataracts
36
facioscapulohumeral dystrophy
face and scapula weakness (triple humps) in shoulder
37
oculopharyngeal muscular dystrophy
ptosis, weakness of eye muscles, prob with swallowing
38
emery-dreifuss muscular dystrophy
contractures
39
becker and dyshen
most common (children)