Peripheral neuropathy Flashcards

1
Q

What happens when the motor part of a large nerve fibre is damaged (in terms of symptoms and effects on power, sensation and reflexes)?

A
  • Symptoms - weakness, unsteadiness and wasting
  • Power - reduced
  • Sensation - normal
  • Reflexes - absent
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2
Q

What happens when the sensory part of a large nerve fibre is damaged (in terms of symptoms and effects on power, sensation and reflexes)?

A
  • Symptoms - numbness, paraesthesia, unsteadiness
  • Power - normal
  • Sensation - vibration and JPS reduced
  • Reflexes - absent
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3
Q

What happens when a small nerve fibre is damaged (in terms of symptoms and effects on power, sensation and reflexes)?

A
  • Symptoms - pain and dysesthesia
  • Power - normal
  • Sensation - pin prick and temperature reduced
  • Reflexes - present
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4
Q

What happens when autonomic fibres are damaged (in terms of symptoms and effects on power, sensation and reflexes)?

A
  • Symptoms - dizziness (postural hypotension), impotence, N+V (gastroparesis)
  • Power - normal
  • Sensation - normal
  • Reflexes - present
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5
Q

What is the name given to nerve root damage?

A

Radiculopathy

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6
Q

What is the name given to nerve plexus injury?

A

Plexopathy

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7
Q

What is the name given to injury to a peripheral nerve?

A

Peripheral neuropathy, which encompasses; mononeuropathy and mononeuritis multiplex

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8
Q

What are some causes of demyelinating neuropathy?

A
  • Acute (days to weeks) - Guillaine Barre syndrome
  • Chronic (months to years) - chronic inflammatory demyelinating polyradiculopathy (CIDP), hereditary sensory motor neuropathy (Charcot-Marie-Tooth disease)
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9
Q

How does Guillain-Barre syndrome typically present?

A
  • 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
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10
Q

How is Guillain-Barre syndrome treated?

A
  • Immunoglobulin infusion and/or plasma exchange
  • 25% require mechanical ventilation
  • 10% die mainly from autonomic failure (cardiac arrhythmia)
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11
Q

What is hereditary neuropathy and how does it present? *apparently common in exams*

A
  • 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
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12
Q

Name some examples of axonal neuropathies

A
  • 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
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13
Q

Name some causes of autonomic neuropathy

A
  • Chronic - diabetes, amyloidosis, hereditary
  • Acute - GBS, porphyria
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14
Q

How are axonal neuropathies treated?

A
  • Treat cause
  • Symptomatic treatment - physiotherapy, orthotics, neuropathic pain relief
  • Vasculitic cause - pulsed IV methylprednisolone + cyclophosphamide
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15
Q

How are demyelinating neuropathies treated?

A

IV Ig, steroids, azathioprine, mycophenalate, cyclophosphamide

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