10.11.3 Peripheral Neuropathies Flashcards

1
Q

Classify polyneuropathies

A

Acute/subacute polyneuropathies
- Time to nadir
— < 4 weeks: acute
— 4-12 weeks: subacute
- Often reversible

Chronic polyneuropathies
- Time to nadir > 12 weeks —
- Often not reversible

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2
Q

Causes of acute polyneuropathy

A
  • Guillain-Barré syndrome
  • Porphyria
  • Thiamine deficiency neuropathy
  • Severe hyperkalaemia
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3
Q

Causes of subacute polyneuropathies

A
  • Thiamine deficiency neuropathy
  • Paraneoplastic neuropathy
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4
Q

Causes of chronic polyneuropathies

A
  • Diabetic polyneuropathy
  • Toxic polyneuropathies (Alcohol; Medications)
  • HIV infection
  • Inflammatory (CIDP;Paraproteinemic)
  • Nutritional / vitamin deficiencies
  • Hereditary
  • Other systemic diseases (Chronic renal failure)
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5
Q

Symptoms of polyneuropathies

A

Symptoms
- Sensory: numbness, paresthesias, pain, ̄ temperature or pain
sensation
- Motor: weakness, clumsiness, incoordination

Signs
- Distal sensory loss, distal weakness, distal reflex loss

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6
Q

Guillian-Barré Syndrome - acute/ subacute polyneuropathies
Pathogenesis
Types x2

A

Post-infectious illness:
- Respiratory tract or GIT
- 3 days - 6 weeks after infection
- Reported by 2/3 patients
- Mechanism: “molecular mimicry”

1. AIDP - Acute inflammatory demyelinating polyneuropathy
- Inflammatory attack on myelin sheath
- Commonest form of GBS (± 90%) —

2. Axonal forms (AMAN & AMSAN)
- Antibody-mediated attack at nodes of Ranvier
- About 10% of cases

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7
Q

Guillian-Barré Syndrome
Clinical

A
  • Proximal and distal weakness with areflexia (absent reflexes)
  • No / minimal sensory symptoms
  • Usually no sphincter dysfunction
  • Cranial nerve dysfunction —
    ➡️Most often facial weakness
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8
Q

GBS and HIV infection

A
  • GBS more common in HIV-infected people
  • Clinical features similar
  • CSF findings similar, except for the presence of up to ± 100 lymphocytes
  • Treatment similar
  • Outcome appears to be similar
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9
Q

GBS outcome

A

2-8% mortality rate

Survivors:
- 70 % recover completely / minimal symptoms
- 20% unable to run
- 8% unable to walk unassisted —
- 2% bedridden

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10
Q

Porphyria

A
  • Group of inherited disorders of haem synthesis

Clinically
- Abdominal pain
- ± skin lesions
- Seizures and delirium
- Polyneuropathy with global weakness — (Acute intermittent porphyria; Porphyria variegata)

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11
Q

Paraneoplastic neuropathy

A
  • Subacute sensory (ataxic) (or sensorimotor) neuropathy —
  • Not painful
  • Often presents before the cancer
  • Thus:
    — Subacute sensory neuropathy: aggressive search for cancer
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12
Q

Diabetic polyneuropathy
General
Clinical features
Complications

A
  • ⬆️ incidence with ⬆️ duration of diabetes

Clinical features
- Insidious onset of numbness, paresthesias, burning pain, hyperesthesia
- Slow progression over years
- Starts distally, progresses proximally
- Sensory complaints most frequent
- Motor involvement (less frequent and later)
- Often associated carpal tunnel syndrome

Sensory loss may lead to
- Repetitive trauma to skin, bone, joints (Charcot joints) —
- Impaction of foreign objects
- Foot ulcers
- Sepsis

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