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HTLV-1-associated demyelinating neuropathy: A case report and review of the literature

A 78-year-old man developed paresthesias in the extremities. He was referred to our hospital because of positive anti-human T-cell leukemia virus type 1 (HTLV-1) antibodies in the serum and the presence of abnormal lymphocytes. He was diagnosed as chronic-type adult T-cell leukemia/lymphoma. Neurolo...

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Detalles Bibliográficos
Autores principales: Tamaki, Keiko, Mishima, Takayasu, Tateishi, Yuji, Mera, Hidekazu, Ogura, Hiromu, Tsugawa, Jun, Fujioka, Shinsuke, Takamatsu, Yasushi, Tsuboi, Yoshio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9986509/
https://www.ncbi.nlm.nih.gov/pubmed/36891478
http://dx.doi.org/10.1016/j.ensci.2023.100453
Descripción
Sumario:A 78-year-old man developed paresthesias in the extremities. He was referred to our hospital because of positive anti-human T-cell leukemia virus type 1 (HTLV-1) antibodies in the serum and the presence of abnormal lymphocytes. He was diagnosed as chronic-type adult T-cell leukemia/lymphoma. Neurological examination revealed sensory impairment in the distal parts of the extremities with loss of deep tendon reflexes. Nerve conduction study showed motor and sensory demyelinating polyneuropathy, indicating a diagnosis of HTLV-1-associated demyelinating neuropathy. Corticosteroid therapy followed by intravenous immunoglobulin therapy improved his symptoms. Since demyelinating neuropathy associated with HTLV-1 infection is not well recognized, we here report its characteristics and clinical course through our case report and literature review.