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Adult T-cell leukemia in Japan.

Authors :
Takatsuki K
Matsuoka M
Yamaguchi K
Source :
Journal of acquired immune deficiency syndromes and human retrovirology : official publication of the International Retrovirology Association [J Acquir Immune Defic Syndr Hum Retrovirol] 1996; Vol. 13 Suppl 1, pp. S15-9.
Publication Year :
1996

Abstract

Adult T-cell leukemia (ATL) was first reported in Japan, where it has a high incidence in the southwestern region. The retrovirus, human T-lymphotropic virus type I (HTLV-I), is found to be the causative agent of ATL. In ATL-endemic areas, the rate of HTLV-I carriers is high. A definite diagnosis of ATL is based on the presence of HTLV-I proviral DNA in the tumor cell DNA. ATL cells originate from the CD4 subset of peripheral T cells. ATL shows diverse clinical features but can be divided into four subtypes: the acute, chronic, smoldering, and lymphoma types. Chemotherapy is not effective; the acute and lymphoma types have a poor prognosis. Familial occurrence of ATL is common. HTLV-I infection is caused by transmission of live infected lymphocytes from mother to child, or from man to woman, or by blood transfusion.

Details

Language :
English
ISSN :
1077-9450
Volume :
13 Suppl 1
Database :
MEDLINE
Journal :
Journal of acquired immune deficiency syndromes and human retrovirology : official publication of the International Retrovirology Association
Publication Type :
Academic Journal
Accession number :
8797698
Full Text :
https://doi.org/10.1097/00042560-199600001-00004