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On the discovery of a new clinical entity: Human T-cell lymphotropic virus Type I-associated Myelopathy (HAM). Mitsuhiro OSAME 1 , Akihiro IGATA 1 , Makoto MATSUMOTO 2 , Koichiro USUKU 1 , Isao KITAJIMA 1 , Kanehisa TAKAHASHI 1 1Third Department of Internal Medicine, School of Medicine, Kagoshima University 2Institute of Cancer Research, School of Medicine, Kagoshima University pp.727-745
Published Date 1987/10/10
DOI https://doi.org/10.11477/mf.1431905922
  • Abstract
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The history of HTLV-I-associated myelopathy (HAM) dates back 15 years ago when one of us (Professor Igata) started his new department in Kagoshima Prefecture, whereupon he pointed out some peculiarities of spinal spastic paraplegia (SSP) cases in this locale. Specifically, not only was the incidence high but also that cases tended to have clusters of characteristic neurologic features. These signs and symptoms were: slowly progressive clinical course, prominent pyramidal tract signs and mild sensory and sphincteric disturbances. In 1975, one of us (M. Osame) showed through an epidemiologic study in the same locale, that of the 1,700,000 population, 55 cases were SSP compared to the 29 Duchenne Dystrophy cases. Retrospetive study of the sporadic SSP cases revealed that majority of them were in fact HAM.


Copyright © 1987, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 1882-1243 印刷版ISSN 0001-8724 医学書院

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