spinal cord lesions Flashcards

1
Q

diseases that affect motor neurons in anterior horn (LMN diseases)

A

poliovirus
west nile virus
spinal muscular atrophy (Werdnig Hoffman disease)

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2
Q

AR disease
neuron death in anterior horn of spinal cord
infant: flaccid paralysis, die

A

spinal muscular atrophy (Werdnig Hoffman disease)

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3
Q

disease affects oligodendroglia (CNS) →
demyelination of CNS (no saltatory conduction) →
random and symmetric lesions in white matter of spinal cord + brainstem + brain
`

A

multiple sclerosis

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4
Q
autoimmune disease
more common in women 20-30 yo
charcot's triad: 
scanning speech
intention tremor
nystagmus
may also have: 
internuclear opthalmoplegia (lesion to MLF) - paralysis of adducting eye + nystagmus of abducting eye on attempted lateral gaze 
bowel/bladder incontinence
optic neuritis
A

multiple sclerosis

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5
Q

CSF of poliovirus

A

lymphocytic pleocytosis

N/slight elevation of protein

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6
Q

CSF of multiple sclerosis

A

very HIGH elevation of protein (immunoglobulin light chains = oligoclonal bands on electrophoresis)

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7
Q

diagnosis of MS

A

lesions of brain + spinal cord

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8
Q

treatment of MS

A

severe exacerbation: high dose steroids for 1 week
IFN-B
natalizumab
if bladder incontinence/neurogenic bladder: catheter
spastistity (no UMN): muscular relaxer
pain: opioids

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9
Q

disease that affects motor neurons of anterior horn (LMN) + lateral corticospinal tracts (UMN)

A

amyotrophic lateral sclerosis (ALS)

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10
Q
LMN signs  + UMN signs (no sensory deficit)
rapidly progressive weakness
muscle atrophy
fasiculations
spasticity
difficulty speaking (dysarthria)
difficulty swallowing (dysphagia)
difficulty breathing (dyspnea)
A

amyotrophic lateral sclerosis (ALS)

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11
Q

defect in superoxide dismutase 1

A

amyotrophic lateral sclerosis (ALS)

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12
Q

treatment of ALS

A

↑ survival time: Riluzole: ↓ presynaptic glutamate release since neurotoxic at high doses

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13
Q

3° syphilis causes

A

tabes dorsalis

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14
Q

disease with no dorsal columns: no light touch + proprioception
+ Romberg sign (need 2 of 3 variables to maintain balance - no visual + proprioception)
argyll robertson pupil
absent DTR
sensory ataxia at night: broad-gait

A

tabes dorsalis (3° syphilis)

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15
Q

Argyll Robertson pupil

A

pupil accommodates but doesn’t react to light (3° syphilis - tabes dorsalis)

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16
Q

loss of pain + temp sensation (spinothalamic)
loss of bilateral motor command: corticospinal tracts (UMN signs) + anterior horns (LMN signs)
BELOW lesion: complete motor paralysis, loss of pain + temp, areflexia

A

anterior spinal artery lesion (only spares dorsal columns + Lissauer’s tracts - light pressure, touch, vibration)

17
Q

cause of anterior spinal artery lesion

A

aortic aneurysm
aortic dissection
direct trauma to aorta
atherosclerosis

18
Q

cyst (syrinx) or cavity within spinal cord

usually between C2-T9

A

syringomyelia

19
Q

associated with Chiari malformation I

A

syringomyelia

20
Q

most commonly affects: C2-T9
damage to anterior white commisure + spinothalamic tracts
+/- chronic pain
may lose sensations in hands

A

syringomyelia

dorsal columns: fine touch proprioception spared

21
Q

complete hemisection of spinal cord:
below lesion:
ipsilateral UMN signs (no corticospinal tract)
ipsilateral loss of tactile, vibration, proprioception (no dorsal columns)
CONTRALATERAL loss of pain + temperature 2-3 (no corticospinal tracts) segments BELOW lesion
At lesion:
ISPILATERAL pain + temp loss for 2-3 segments (no Lissauer tract)
ipsilateral LMN signs (no anterior horn)

A

brown-sequard syndrome

22
Q

CSF of Guillain-Barre syndrome

A

↑ protein

normal cell count