Neuro II Lecture 5 - ALS/GBS/Sensation Flashcards

1
Q

what is somatosensation

A

sensation received from skin and musculoskel system

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2
Q

what is proprioception

A

position sense

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3
Q

what is pallesthesia

A

vibration sense

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4
Q

what is stereognosis

A

object recognition

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5
Q

what is topognosis

A

tactile recognition

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6
Q

what does the anterolateral spinothalamic system detect?

A

pain and temp

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7
Q

what does the DCML detect

A

proprioception
vibration
2-point
stereognosis

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8
Q

how do you begin sensory testing?

A

distal to proximal, bilaterally
random sequence and pace
vision occluded

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9
Q

superficial sensory receptors detect what

A

pain, temp, light touch, pressure

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10
Q

deep sensory receptors detect what

A

position sense, kinesthesia, vibration

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11
Q

combined cortical sensation receptors detect what

A

stereognosis, two point, barognosis, graphesthesia, tactile localization, recognition of texture, double simultaneous stimulation

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12
Q

What is the pathology for Guillain-Barré Syndrome?

A

spinal roots and peripheral nerves are infiltrated with macrophages and T-lymphocytes, attack/strip myeline sheaths (milder cases have intact axons and can re-myelinate)

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13
Q

What are the clinical characteristics of Guillain-Barré Syndrome?

A

rapid progression of weakness and sensory changes starting symmetrically distally progressing proximal. Absent/diminished reflexes, flaccid paralysis

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14
Q

What is the progression of Guillain-Barré Syndrome?

A

progression of symtpoms generally stops within 2-4 weeks, then a static/all time low phase beings for another 2-4 weeks, recovery(ranging from months-years) occurs in a proximal to distal pattern

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15
Q

What is required for a Guillain-Barré Syndrome diagnosis?

A

loss of DTRs, progressive weakness in more than one extremity // in order of importance: rapid symmetric weakness plateauing around 4 weeks, mild sensory changes, facial weakness, recovery starts within 2-4 weeks, tachycardia/arrhythmyias/varying BP, NO fever

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16
Q

What is the prognosis for Guillain-Barré Syndrome?

A

good prognosis, slow rate of peripheral nerve recovery at 1-2mm or 0.04-0.08in / day (1-2in/month)

17
Q

What factors predict a poor outcome for Guillain-Barré Syndrome?

A

older age onset, longer time before recovery begins, need for ventilation, indicated axonal degeneration

18
Q

does ALS have UMN or LML involvement

A

both

19
Q

what tests are done to “rule in” or diagnose ALS

A

clinical exam
motor only, progression of sx, UMNL and LMNL

20
Q

what tests are done to “rule out” ALS

A

imaging of brain/spine
blood tests
CSF sample
muscle biopsy

21
Q

What is Amyotrophic Lateral Sclerosis?

A

a degenerative terminal disease affecting BOTH upper and lower motor neurons

22
Q

What structures are affected in ALS?

A

the cortex, corticospinal tract, brainstem nuclei of CN V, VII, IX, X, and XII, and anterior horn cells in spinal cord

23
Q

How is ALS diagnosed?

A

LMN and UMN lesions found by clinical examination + progression of disease within a region(s) AND an absence of any evidence that may indicate another disease

24
Q

how does ALS present

A

UMNL+LMNL
no sensory changes
progressive/fatal
asymmetric