Peripheral Neuropathy Flashcards

1
Q

does MS cause peripheral neuropathy

A

no

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2
Q

loss of reflexes means a problem where

A

peripheral nerves- large motor or sensory fibres

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3
Q

which type of fibres conduct the slowest

A

C- unmyelinated

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4
Q

what do Aalpha fibres do

A

motor- muscle control

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5
Q

what do large sensory Aalpha/ beta fibres do

A

touch, vibration, position perception

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6
Q

what do thinly myelinated Adelta sensory fibres do

A

cold perception

pain

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7
Q

what do un myelinated C sensory fibres do

A

warm perception

pain

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8
Q

what are the type of autonomic nerve fibres

A

Adelta- thinly myelinated

C- unmyelinated

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9
Q

what are the symptoms when a large motor fibre is affected

A

weakness, unsteadiness, wasting

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10
Q

what are the symptoms when a large sensory fibres is affected

A

numbness
paraesthesia
unsteadiness

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11
Q

what are the symptoms when a small sensory fibre is affected

A

pain dyesthesia (painful itchy sensation)

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12
Q

what are the symptoms when autonomic fibres are affected

A

dizziness due to postural hypotension
impotence
nausea and vomiting (gastroparesis)

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13
Q

what peripheral fibres are affected when there is reduced power

A

large motor fibres (Aalpha)

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14
Q

what fibres are affected when there is reduced vibration and joint position sensation

A

large sensory (Aalpha/beta)

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15
Q

what fibres are affected when there is reduces pin prick and temperature sensation

A

small sensory fibre (Adelta/ C)

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16
Q

what is pseudoathetosis

A

abnormal writhing movement (usually of the fingers) due to failure of proprioception

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17
Q

what does a high stepping gate result from

A
foot drop due to weakness of ankle dorsiflexion
DDx
-peroneal palsy 
-L5 root lesion 
-motor neuropathy
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18
Q

what is damages in a radiculopathy

A

nerve root

19
Q

what commonly causes radioculopathy

A

prolapse

can be inflammatory

20
Q

what is damaged in plexopathy

A

plexus

21
Q

what is peripheral neuropathy

A

damage to the nerve distal to the plexus

22
Q

what are the types of peripheral neuropathy

A

mononeuropathy (single nerve, e.g trauma)
mononeuritis multiplex (progressive sensory or motor deficits in a specific distribution of peripheral nerves caused by systemic illness- vasculitis, hypersensitivity, drugs etc)
length dependent peripheral neuropathy- small fibre
polyneuropathy- symmetrical distribution

23
Q

what is the distribution of length dependent peripheral neuropathy

A

glove and stocking, usually symmetrical

24
Q

what is the most common type of peripheral neuropathy

A

length dependent

25
Q

what is symmetrical wasting suggestive of

A

PN, if asymmetrical less likely

26
Q

what is the pattern of loss in mononeuritis/ mononeuropathy

A

loose function very quickly (blood supply lost due to inflammation)
asymmetrical
patchy sensory loss

patient can present with e.g. wrist drop/ foot drop

27
Q

what is the pattern of loss in radiculopathy

A

loss of reflex and muscle function

asymmetrical

28
Q

what most commonly causes a plexoathy

A

traction injury

29
Q

how can peripheral nerves be damaged

A

axonal loss

demyelination (not MS)

30
Q

what results from a demyelinating neuropathy

A

conduction is slowed

31
Q

what causes an acute (days to weeks) demyelinating neuropathy

A

guillaine barre syndrome

32
Q

what causes a chronic (months to years) demyelinating neuropathy

A

chronic inflammatory demyelinating polyradiculopathy

hereditary sensory motor neuropathy (used to be called charcot marie tooth disease)

33
Q

what is the presentation and duration of GBS like

A

progressive paraplegia over days lasts up to four weeks
peak symptoms at 10-14 days
associated sensory symptoms (pain very common) proceed weakness

34
Q

what infection is associated with GBS

A

campylobacter

-inflammation of axon- stripped myelin

35
Q

what is the prognosis of GBS

A

25% require ventilation

10% die form autonomic failure (cardiac arrythmia)

36
Q

what is the treatment for GBS

A

immunoglobulin infusion and/ or plasma exchange

37
Q

what is exam like in GBS

A

initially reflexes will be normal, as they ‘ go off legs’ may loose them

38
Q

what are the hereditary neuropathies

A

pure motor, sensory, sensorimotor, small fibre and autononmic variants
can be demyelinating or axonal
AD, AR, X linked types

39
Q

what happens in the HMSN type 1 hereditary neuropathy

A

longstanding loss of muscle, pes cavus, thin distal musculature

40
Q

what are the types of axonal neuropathies

A

idiopathic (age related)
vasculitis (mononeuritis multiplex)
paraneoplastic
infectious (HIV, syphillis, lyme, hepatitis)
drugs/ toxins
metabolic (diabetes, B12/ folate, hypothyroidism)

41
Q

what are the causes of chronic autonomic neuropathy

A

diabetes (gastroparesis)
amyloidosis
hereditary

42
Q

what are the acute causes of autonomic neuropathy

A
GBS
porphyria (unexplained abdo pain in the young)
43
Q

what is the treatment for axonal peripheral neuropathy

A
treat cause e.g. infection 
symptomatic relief (physio, orthotics, neuropathic pain relief)

if vasculitic
pulsed IV meythlprednisolone + cyclophosphamide

44
Q

what is the treatment for demyelinating peripheral neurpathies

A

IV immunoglobulins
steroids
azathioprine, mycophenalate, cyclophosphamide