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[Paraplegia associated with HTLV 1 in Martinique. Study of 271 cases including 70 with neuromuscular involvement]

D Smadja1, P Cabre, R Bellance

  • 1Service de neurologie, Hôpital Pierre Zobda-Quitman, Fort-de-France.

Insights

Human T-lymphotropic virus type 1 (HTLV1) causes a variable myelopathy in Martinique, often accompanied by neurological and systemic symptoms. Early detection and management are crucial for patients with HTLV1-associated myelopathy.

Area of Science:

  • Neurology
  • Infectious Diseases
  • Epidemiology

Context:

  • Human T-lymphotropic virus type 1 (HTLV1) infection is endemic in Martinique.
  • HTLV1-associated myelopathy (HAM) is a significant neurological complication in the region.
  • A substantial number of cases have been documented, highlighting the public health burden.

Purpose:

  • To describe the clinical spectrum and progression of HTLV1-associated paraplegia in Martinique.
  • To investigate the frequency and nature of neuromuscular involvement.
  • To document the prevalence of extra-neural manifestations associated with HTLV1.

Summary:

  • 271 cases of HTLV1-associated paraplegia were identified in Martinique.
  • Clinical presentation commonly includes spastic paraparesis/paraplegia, sphincter disturbances, and lower limb pain.
  • Disease severity varies, with a significant proportion experiencing mobility impairment over time.
  • Neuromuscular involvement (e.g., amyotrophy, myositis) and extra-neural spread (e.g., alveolitis, sicca syndrome) are frequent.

Impact:

  • Provides crucial epidemiological data on HTLV1-associated myelopathy in a specific geographic area.
  • Highlights the diverse clinical manifestations, aiding in diagnosis and patient management.
  • Emphasizes the systemic nature of HTLV1 infection beyond neurological symptoms.
  • Informs public health strategies for prevention and control of HTLV1 in endemic regions.

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