Peripheral neuropathy Flashcards
What happens when the motor part of a large nerve fibre is damaged (in terms of symptoms and effects on power, sensation and reflexes)?
- Symptoms - weakness, unsteadiness and wasting
- Power - reduced
- Sensation - normal
- Reflexes - absent
What happens when the sensory part of a large nerve fibre is damaged (in terms of symptoms and effects on power, sensation and reflexes)?
- Symptoms - numbness, paraesthesia, unsteadiness
- Power - normal
- Sensation - vibration and JPS reduced
- Reflexes - absent
What happens when a small nerve fibre is damaged (in terms of symptoms and effects on power, sensation and reflexes)?
- Symptoms - pain and dysesthesia
- Power - normal
- Sensation - pin prick and temperature reduced
- Reflexes - present
What happens when autonomic fibres are damaged (in terms of symptoms and effects on power, sensation and reflexes)?
- Symptoms - dizziness (postural hypotension), impotence, N+V (gastroparesis)
- Power - normal
- Sensation - normal
- Reflexes - present
What is the name given to nerve root damage?
Radiculopathy
What is the name given to nerve plexus injury?
Plexopathy
What is the name given to injury to a peripheral nerve?
Peripheral neuropathy, which encompasses; mononeuropathy and mononeuritis multiplex
What are some causes of demyelinating neuropathy?
- Acute (days to weeks) - Guillaine Barre syndrome
- Chronic (months to years) - chronic inflammatory demyelinating polyradiculopathy (CIDP), hereditary sensory motor neuropathy (Charcot-Marie-Tooth disease)
How does Guillain-Barre syndrome typically present?
- Progressive paraplegia over days up to 4 weeks
- Associated sensory symptoms proceed weakness
- Pain is very common!
- Peak symptoms are 10-14 days into onset of illness
- Examination can be normal in the initial phases of illness
How is Guillain-Barre syndrome treated?
- Immunoglobulin infusion and/or plasma exchange
- 25% require mechanical ventilation
- 10% die mainly from autonomic failure (cardiac arrhythmia)
What is hereditary neuropathy and how does it present? *apparently common in exams*
- Autosomal dominant or recessive or X-linked - hundreds of mutations
- Pure motor, sensory, sensorimotor, small fibre and autonomic variants
- Demyelinating and axonal varieties
- Genetic testing available for the most common mutations e.g. CMT1a
Name some examples of axonal neuropathies
- Idiopathic
- Vasculitic - ANCA+ve, rheumatoid arthritis, Sjogren’s syndrome
- Paraneoplastic - myeloma, breast cancer
- Infections - HIV, syphilis, lyme
- Drugs - alcohol, amiodarone, phenytoin
- Metabolic - diabetes, B12/folate deficiencies, hypothyroidism, chronic uraemia, porphyria
Name some causes of autonomic neuropathy
- Chronic - diabetes, amyloidosis, hereditary
- Acute - GBS, porphyria
How are axonal neuropathies treated?
- Treat cause
- Symptomatic treatment - physiotherapy, orthotics, neuropathic pain relief
- Vasculitic cause - pulsed IV methylprednisolone + cyclophosphamide
How are demyelinating neuropathies treated?
IV Ig, steroids, azathioprine, mycophenalate, cyclophosphamide