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Update on Neurological Manifestations of HTLV-1 Infection

  • Central Nervous System Infections (J Lyons, Section Editor)
  • Published:
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Abstract

The human T cell lymphotropic virus type 1 (HTLV-1) is a retrovirus that infects 10–20 million persons around the world. Initially associated with the hematological malignancy adult T cell leukemia/lymphoma (ATLL), HTLV-1 is also the cause of a chronic progressive myelopathy named “HTLV-1-associated myelopathy/tropical spastic paraparesis” (HAM/TSP). HAM/TSP arises as the tip of the iceberg of an assortment of neurological syndromes triggered by the virus such as inflammatory myopathies, polyneuropathies, amyotrophic lateral sclerosis (ALS)-like syndromes, dysautonomia, and cognitive impairment. HAM/TSP typifies a chronic progressive spastic paraparesis with neurogenic bladder and minimal sensory signs. The neuropathology of HAM/TSP is concentrated in the thoracic spinal cord and is typically biphasic. Initially, there is a perivascular lymphocytic cuffing and mild parenchymal mononuclear infiltrates. Subsequently, this is replaced by gliosis and scarring. The neuropathogenesis of HTLV-1 is still partially understood. At present, the therapy of HAM/TSP remains basically symptomatic.

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Abelardo Araujo has no disclosures.

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Correspondence to Abelardo Q-C Araujo.

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This article is part of the Topical Collection on Central Nervous System Infections

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Araujo, A.QC. Update on Neurological Manifestations of HTLV-1 Infection. Curr Infect Dis Rep 17, 6 (2015). https://doi.org/10.1007/s11908-014-0459-0

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