Peripheral Neuropathy Flashcards

(30 cards)

1
Q

features of large motor fibre damage?

A
weakness
unsteadiness
wasting
reduced power
normal sensation
absent reflexes
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2
Q

features of large sensory fibre damage?

A
numbness
paraesthesia
unsteadiness
normal power
vibration and JPS reduced
absent reflexes
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3
Q

features of small fibre damage?

A
pain
dyesthesia
normal power
pin prick and temperature sensation reduced
reflexes present
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4
Q

features of autonomic nerve damage?

A
dizziness
impotence
nausea and vomiting
normal power
normal sensation
reflexes present
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5
Q

types of motor fibre?

A

myelinated A alpha

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6
Q

sensory fibres?

A
myelinated A alpha/beta (touch, vibration, proprioception)
thinly myelinated A delta (cold, pain)
unmyelinated C (heat, pain)
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7
Q

autonomic fibres?

A

thinly myelinated A delta

unmyelinated C fibres

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8
Q

pseudoathetosis?

A

due to loss of proprioception (A alpha/beta fibres)

causes writhing hand motion when eyes are closed

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9
Q

radiculopathy?

A

nerve root is damaged

- most common cause = disc prolapse but can be an inflammatory cause

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10
Q

plexopathy?

A

damage in plexus

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11
Q

peripheral neuropathy?

A

damage to peripheral nerve

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12
Q

3 examples of types of peripheral neuropathy?

A
mononeuropathy (e.g wrist drop)
mononeuritis multiplex (lost of nerves picked off)
length dependant peripheral neuropathy
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13
Q

length dependant peripheral neuropathy?

A

weakness/sensory loss in length dependant pattern

classic glove and stocking pattern but can be more severe and spread to more central areas

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14
Q

symmetrical vs asymmetrical wasting in muscle?

A
symmetrical = more likely to be length dependant peripheral neuropathy
asymmetrical = more likely to be compression on single nerve (carpal tunnel/compression by tumour) or something worse like MND
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15
Q

what is mononeuritis multiplex?

A

associated with vasculitis
asymmetrical patchy neuropathy in context of other illness
lots of nerve affected

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16
Q

radiculopathy follows what pattern?

A

spinal nerve dermatomes and myotomes

17
Q

most common plexopathy?

A

traction injury in arm (e.g erbs palsy)

18
Q

presentation of plexopathy?

A
often have a lot of pain
widespread symptoms (e.g whole limb)
19
Q

old people vs young people with nerve damage?

A
old = axonal loss
young = demyelination (e.g guillan barre)
20
Q

neurophysiology?

A

testing which can determine whether axonal loss of demyelination

21
Q

features of demyelinating neuropathy?

A

acute (days to weeks)
- e.g Guillaine barre syndrome or AIDP)
chronic (months to years)
- CIDP (chronic inflammatory demyelinating polyradiculopathy)
- hereditary sensory motor neuropathy neuropathy (AKA charcot-Marie-Tooth disease)

22
Q

what is GBS?

A

progressive paraplegia over days up to 4 weeks
associated sensory symptoms precedes weakness
can be fairly normal initially then go “off legs” and loose reflexes
often after illness/infection
pain very common
peak symptoms 10-14 days into illness
can have normal examination initially

23
Q

how is GBS managed?

A

IV immunoglobulin infusion and/or plasma exchange

24
Q

cause of death in GBS?

A

autonomic failure (cardiac arrhythmia)

25
what is hereditary neuropathy?
AD, AR, X linked pure motor, sensory, sensorimotor..... …. typically have wasted (champagne bottle deformity) of tibial muscles deforming arthropathy of hands and feet (e.g pes cavus)
26
types of axonal neuropathy?
idiopathic vasculitis (likely to cause disability?) paraneoplastic infections (HIV, syphilis, lyme, hepatitis) drugs/toxins (alcohol, amiodarone, phenytoin, chemo) metabolic (diabetes, hypothyroid)
27
chronic autonomic neuropathy?
diabetes (gastroparesis) amyloidosis hereditary
28
acute autonomic neuropathy?
GBS | porphyria
29
treatment of axonal peripheral neuropathy?
``` treat cause symptomatic treatment (physio, orthotics, neuropathic pain relief) ```
30
how can radiculopathy and peripheral nerve compression be differentiated?
radiculopathy = shooting pains