What are the clinical manifestations of leprosy (Hansen disease)?

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Signs and Symptoms of Leprosy (Hansen Disease)

Cardinal Clinical Features

Leprosy diagnosis requires one or more of three cardinal signs: hypopigmented or erythematous skin patches with definite loss of sensation, thickened peripheral nerves, and acid-fast bacilli on skin smears or biopsy. 1

Skin Manifestations

Tuberculoid (Paucibacillary) Form

  • One or few well-demarcated, hypopigmented skin lesions with active spreading edges and clearing centers 2, 3
  • Lesions demonstrate complete anesthesia (loss of sensation) which is pathognomonic for leprosy 4
  • Peripheral nerve swelling may be palpable near affected skin areas 3

Lepromatous (Multibacillary) Form

  • Multiple erythematous papules and nodules with bilateral and symmetrical distribution affecting face, hands, and feet 2, 4
  • Diffuse skin infiltration progressing to skin thickening with loss of normal skin architecture 4
  • Nodules (lepromas) develop and may ulcerate 4
  • Lesions range from porcelain-white to erythematous coloration 4

Neurological Manifestations

  • Peripheral nerve damage is the hallmark complication, with M. leprae primarily infecting Schwann cells 1
  • Thickened peripheral nerves are palpable on examination 3, 1
  • Sensory loss in affected skin areas, particularly in hands and feet 5
  • Weakness and numbness in extremities 5
  • "Silent neuropathy" may occur where nerves are functionally impaired before obvious symptoms develop 6

Upper Respiratory Involvement

  • Nasal symptoms from upper respiratory mucosa involvement 3
  • Nasal stuffiness or epistaxis may occur in lepromatous disease 2

Ocular Manifestations

  • Eye pain or loss of vision from direct ocular involvement 5
  • Lagophthalmos (inability to close eyelids) from facial nerve damage 6

Disease Spectrum Characteristics

The clinical presentation exists on a spectrum based on host T-cell-mediated immune response to M. leprae 2, 6:

  • Tuberculoid pole: Strong cellular immunity, few lesions, low bacterial load 2
  • Lepromatous pole: Weak cellular immunity, multiple lesions, high bacterial load 2
  • Borderline forms: Intermediate presentations between the two poles 3

Critical Diagnostic Pitfalls

  • In non-endemic areas, leprosy is frequently misdiagnosed as tinea versicolor, vitiligo, or other common dermatoses because clinicians fail to consider it 7
  • Anesthesia in skin lesions distinguishes leprosy from most mimics and must be actively tested 4
  • Early recognition is crucial as nerve damage is irreversible once established 8
  • Patients from endemic areas (Brazil, India, Southeast Asia, Africa) presenting with hypopigmented patches warrant high suspicion 7

Immunologic Reactions

  • Type 1 reversal reactions: Acute inflammation in existing lesions with increased erythema and edema 6, 5
  • Type 2 reactions (erythema nodosum leprosum): Painful subcutaneous nodules, fever, and systemic symptoms 6, 5
  • These reactions can occur before, during, or after treatment and represent immune-mediated exacerbations requiring prompt corticosteroid therapy while continuing antibacterial treatment 5

References

Research

Leprosy: an overview of pathophysiology.

Interdisciplinary perspectives on infectious diseases, 2012

Guideline

Leprosy Diagnosis and Treatment

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Hansen's Disease (Leprosy): Clinical Presentation and Diagnosis

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Lepromatous Leprosy Diagnosis and Differential Diagnoses

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Research

[Neurological manifestations of leprosy].

Revue neurologique, 2003

Research

A case of Hansen Disease presenting as tinea versicolor.

Dermatology online journal, 2013

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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