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日本的成人T细胞白血病

Adult T-cell leukemia in Japan.

作者信息

Takatsuki K, Matsuoka M, Yamaguchi K

机构信息

Kumamoto University School of Medicine, Japan.

出版信息

J Acquir Immune Defic Syndr Hum Retrovirol. 1996;13 Suppl 1:S15-9. doi: 10.1097/00042560-199600001-00004.

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.

摘要

成人T细胞白血病(ATL)最早在日本被报道,该国西南部地区发病率较高。逆转录病毒——人类T淋巴细胞白血病病毒I型(HTLV-I)——被发现是ATL的致病因子。在ATL流行地区,HTLV-I携带者比例较高。ATL的确切诊断基于肿瘤细胞DNA中HTLV-I前病毒DNA的存在。ATL细胞起源于外周T细胞的CD4亚群。ATL表现出多样的临床特征,但可分为四种亚型:急性、慢性、冒烟型和淋巴瘤型。化疗无效;急性和淋巴瘤型预后较差。ATL家族性发病很常见。HTLV-I感染是由受感染的活淋巴细胞从母亲传给孩子、或从男性传给女性、或通过输血传播引起的。

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