Management of Painful Neuropathy in Leprosy
Painful neuropathy in leprosy should be treated with a combination of corticosteroids as first-line therapy, followed by anticonvulsants or antidepressants for persistent neuropathic pain. This approach addresses both the inflammatory and neuropathic components of leprosy-related nerve damage.
Pathophysiology and Diagnosis
Leprosy causes nerve damage through:
- Perineural inflammation (hallmark of early leprosy)
- T cell-mediated inflammatory processes
- Direct invasion of Schwann cells by Mycobacterium leprae
- Immune-mediated reactions (Type 1 "Reversal" and Type 2 "ENL")
Diagnosis requires:
- Assessment for sensory loss, motor weakness, and nerve enlargement
- Skin lesions with sensory changes (though pure neuritic forms occur in 10% of cases)
- Nerve conduction studies showing axonal neuropathy patterns
- Nerve biopsy in unclear cases (showing microvasculitis or granulomas)
Treatment Algorithm
Step 1: Control Acute Inflammation
- Corticosteroids (First-line therapy)
Step 2: Manage Persistent Neuropathic Pain
For pain persisting after inflammation control:
- First-line medications:
Anticonvulsants:
- Pregabalin: Start 50-75mg BID, target 300-600mg/day
- Gabapentin: Start 100-300mg daily, target 900-3600mg/day
Antidepressants:
Step 3: Refractory Pain Management
- Second-line options:
- Tramadol (NNT 4.7)
- Consider referral to pain specialist for combination therapy
- Surgical decompression of swollen nerve trunks in select cases 1
Special Considerations
Leprosy Reactional States
Type 1 (Reversal) Reaction:
- Occurs in borderline/tuberculoid leprosy
- Presents with swelling of existing skin and nerve lesions
- Management: High-dose steroids, continue anti-leprosy treatment 1
Type 2 (ENL) Reaction:
- Occurs mainly in lepromatous patients
- Presents with fever, tender erythematous nodules, neuritis
- Management: Steroids, analgesics, continue anti-leprosy treatment 1
Monitoring and Follow-up
- Regular assessment of nerve function (sensory and motor)
- Monitor for steroid side effects
- Long-term follow-up as neuropathy may develop years after successful treatment of infection 5
Important Caveats
- Up to 60% of multibacillary patients have clinically apparent nerve damage at diagnosis
- 30% develop further nerve damage during treatment
- 10% may develop new nerve damage after completing drug treatment 2
- Antibiotics used to treat M. leprae have little effect on nerve damage as it is immune-mediated
- Leprosy Late-Onset Neuropathy (LLON) can occur years (average 19 years) after successful treatment 5
- Neuropathic pain in leprosy is often underrecognized and undertreated 6
Remember that leprosy should be viewed as a chronic neurological condition rather than simply a skin disease 2. Early detection and prompt treatment of nerve involvement are critical to prevent long-term disability, even after successful eradication of the bacteria.