Peripheral neuropathy Flashcards

1
Q

What are the main features of length dependent axonal neuropathy?

A

Numbness starts in toes/feet and works its way up the legs.

Symmetrical and slowly progressive.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What are causes of length dependent axonal neuropathy?

A
Diabetes
Alcohol 
Folate/B12/thiamine deficiency 
Izoniazid, cisplatin, amiodarone 
Pareneoplastic and neoplastic causes
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What is Guillian Barre syndrome?

A

An acute demyelinating inflammatory polyneuropathy.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What can induce GB syndrome?

A

Post infection e.g. campylobacter, CMV, EBV

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What is the pathophys of GB syndrome?

A

Post infection, the immune system thinks myelin is a bit of virus and begins attacking it.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What are the main features in GB syndrome?

A

A progressive ascending weakness over days with flaccis quadraparesis and areflexia.
Can have respiratory, bulbar and autonomic involvement, which can be life-threatening and cause breathing difficulties.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

How is GB treated?

A

Intravenous immunoglobulin or apheresis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

How is chronic inflammatory demyelinating polyneuropathy treated?

A

Steroids and immunoglobulin

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

How is peripheral neuropathy tested for?

A

Nerve conduction studies

  • Myelin damage shows delayed temporal dispersion of impulses e.g. GB
  • Axonal damage shows reduced amplitude.

Also, CSF shows increased protein.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What is myasthenia gravis?

A

An autoimmune disorder mediated by antibodies against acetylcholine receptors at the post-synaptic NMJ.

Can be associated with tumour of residual thymus.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

How does myasthenia gravis present?

A

Fatigue of ocular, bulbar, neck, respiratory, and limb muscles (in that order).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

How is myasthenia gravis tested for?

A

Look for anti-AchR antibodies.

EMG/nerve conduction shows decreasing muscle response to repeated stimulation.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

How is myasthenia gravis treated?

A

Pyridostigmine - anti-acetylcholinesterase to increase Ach levels.

Immunosuppression e.g. prednisolone

How well did you know this?
1
Not at all
2
3
4
5
Perfectly