Demyelination Flashcards

0
Q

Myopathy workup

A
  • EMG: strength may be normal, motor units will be small
  • blood -> elevated CK
  • myopathy confirmed with muscle biopsy/genetic testing
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1
Q

Myopathy presentation

A
  • weakness, often symmetric with NO sensory loss

- inherited: DMD, autoimmune inflammatory: polymyositis, dermatomyocytis

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2
Q

DMD

A
  • myopathy
  • calf hypertrophy (connective tissue)
  • biopsy reveals highly variable fiber size: existing motor unit compensate for decaying ones
  • dystrophin mutation
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3
Q

Inflammatory myopathies

A
  • More common in adults

- presents with proximal weakness and muscle pain

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4
Q

Dermatomyositis

A
  • Grotton’s sign (rash over extensor surface of digits)
  • heliotrope rash on skin exposed to sun
  • perifasciular atrophy
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5
Q

NMJ disease (presentation/diagnosis)

A
  • weakness, no numbness (looks like myopathy)
  • myasthenia gravis most common form lambert eaton second most
  • diagnosis: repetitive stimulation results in decrement or increment
  • ID Abs
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6
Q

Myasthenia gravis vs lambert eaton

A
  • MG: anti-ACh receptor Abs

- LE: anti-presynaptic Ca channels

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7
Q

Myasthenia gravis presentation

A
  • lots of confusing eye stuff (Diplopia, Ptosis)
  • slurred speech
  • dysphagia
  • weakness in arms and legs
  • fatigue
  • difficulty breathing
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8
Q

Generalized neuropathy

A
  • progressive weakness and burning pain -> numbness, often symmetric
  • hyporeflexia
  • often start at feet and ascend
  • Diabeetus, HIV renal failure
  • EMG reveals Large motor units (compensatory resp precedes paralysis)
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9
Q

Trt of diabetic neuropathy

A
  • anticonvulsants: gabapentin/pregabalin
  • SNRIs
  • antidepressants
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10
Q

Diabetic neuropathy: 4 symptoms

A
  • gait problems
  • orthostatic hypotension
  • gastric paresis
  • foot ulcers
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11
Q

Focal neuropathy

A
  • present with numbness and often severe weakness
  • carpal tunnel (nerve compression: compression most common neuropathy) 1st common, ulnar compression 2nd.
  • workup is neuro EMG
  • can result in eventual thenar atrophy
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12
Q

Peroneal nerve pinch

A
Anteriolateral paresthesis
Foot drop (slaps as they walk)
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13
Q

Bell’s palsy

A
  • lesion of CN VII
  • often idiopathic
  • steroids can help
  • recovery typically occurs completely
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14
Q

Radiculopathy

A
  • pain/numbness/tingling in nerve root distribution
  • sometimes weakness
  • usually asymmetric
  • pattern is key
  • biceps: C5/6, triceps: C 7/8, knee: L2/4, ankle: S1/2 (reflex is lost in ridiculopathy)
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15
Q

ALS

A
  • upper and motor neuron signs
  • CSPT AND ventral horn hit
  • EMG will show denervation in all muscle groups
  • diagnosis by rule out: polyrediculopathy
  • can trt (sort of) with glutamate antagonist rulizole
16
Q

Spinal muscular atrophy

A
  • like ALS, but only lower motor neuron signs
  • SMN1 defect
  • 1/6000 are effected; 1/40 are carriers
17
Q

Guillane-barre syndrome (presentation, diagnosis, trt)

A
  • polyneuropathy
  • ascending paralysis
  • EMG and CSF analysis (elevated protein without cells)
  • potential resp compromise
  • IVIg and plasmapheresis