Peripheral Neuropathy Flashcards

1
Q

What are the symptoms of large fibre damage?

A

Motor- weakness, unsteadiness, wasting

Sensory- numbness, paraesthesia, unsteadiness

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2
Q

What are the symptoms of small fibre damage?

A

Pain

Dyesthesia

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3
Q

What are the symptoms of autonomic fibre damage?

A

Dizziness (postural hypotension)
Impotence
Nausea and vomiting (gastroparesis)

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4
Q

What are the changes in power in nerve damage?

A

Large motor- Reduced

Large sensory, small and autonomic- Normal

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5
Q

What are the changes in sensation in large motor and autonomic nerve damage?

A

Normal

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6
Q

What are the changes in sensation in large sensory and small nerve fibres?

A

Large sensory- vibration and JPS reduced

Small- pin prick and temperature reduced

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7
Q

What are the changes in reflexes in nerve damage?

A

Large motor/sensory- Absent

Small/Autonomic- Present

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8
Q

What are some conditions caused by nerve damage specific to location of damage?

A

Radiculopathy
Plexopathy
Peripheral neuropathy- mononeuropathy, mononeuritis multiplex, (length dependant) peripheral neuropathy)

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9
Q

How can peripheral nerves be damaged?

A

Axonal Loss

Peripheral nerve demyelination

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10
Q

What can be used to assess nerve status in demyelinating neuropathies?

A

NCS

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11
Q

What is an acute demyelinating neuropathy?

A

Guillaine Barre/AIDP

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12
Q

What are some chronic demyelinating neuropathies?

A

CIDP (chronic inflammatory demyelinating polyradiculopathy)

Hereditary sensory motor neuropathy (formerly Charcot-Marie-Tooth)

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13
Q

What occurs in GBS?

A

Progressive paraplegia over days up to 4 weeks
Associated sensory symptoms proceed illness
Pain common

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14
Q

When are the peak symptoms of GBS?

A

10-14 days after onset

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15
Q

What can be a cause of GBS?

A

Infection eg. campylobacter

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16
Q

How is GBS treated?

A

Ig infusion and/or plasma exchange (minimal role for steroids)

17
Q

Describe hereditary neuropathies

A

Hundreds of mutations
Pure motor, sensory, sensorimotor, small fibre (congenital insensitivity to pain syndrome) and autonomic variants
Demyelinating and axonal varieties
Genetic testing available for most common

18
Q

What can cause axonal neuropathies?

A
Idiopathic (age related)
Vasculitic
Paraneoplastic
Infections
Drugs/toxins
Metabolic
19
Q

What are the vasculitic (often mononeuritis multiplex) causes of axonal neuropathies?

A

ANCA +ve

Rheumatoid arthritis/Sjrogens syndrome (ANA/ENA +ve)

20
Q

What are the paraneoplastic causes of axonal neuropathies?

A
Myeloma
Antibody mediated (eg breast cancer/SCLC anti hu/yo)
21
Q

What are the infectious causes of axonal neuropathies?

A

HIV
Syphilis
Lyme
Hep B/C (cryoglobulin mediated)

22
Q

What are the drug/toxin-based causes of axonal neuropathies?

A

Alcohol
Amiodarone
Phenytoin
Chemotherapy (cisplatin, vincristine)

23
Q

What are the metabolic causes of axonal neuropathies?

A
Diabetes
B12/folate deficiencies (other)
Hypothyroidism
Chronic uraemia
Porphyria
24
Q

What are some chronic causes of autonomic neuropathy?

A

DM (i.e. gastroparesis)
Amyloidosis
Hereditary

25
Q

What are some acute causes of autonomic neuropathy?

A

GBS

Porphyria

26
Q

What is the treatment of axonal peripheral neuropathy?

A

Treat cause

Symptomatic treatment- physio, orthotics neuropathic pain relief

27
Q

What is the treatment of axonal (vasculitic) peripheral neuropathy?

A

Pulsed IV methylprednisolone + cyclophosphamide

28
Q

What is the treatment of demyelinating (inflammatory) peripheral neuropathy?

A

IVIg (pooled Ig from donors)
Steroids
Azathioprine, mycophenalate, cyclophosphamide