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90例同性恋男性中的非霍奇金淋巴瘤。与全身淋巴结肿大及获得性免疫缺陷综合征的关系。

Non-Hodgkin's lymphoma in 90 homosexual men. Relation to generalized lymphadenopathy and the acquired immunodeficiency syndrome.

作者信息

Ziegler J L, Beckstead J A, Volberding P A, Abrams D I, Levine A M, Lukes R J, Gill P S, Burkes R L, Meyer P R, Metroka C E

出版信息

N Engl J Med. 1984 Aug 30;311(9):565-70. doi: 10.1056/NEJM198408303110904.

Abstract

We describe the histologic and clinical features of non-Hodgkin's lymphoma diagnosed between January 1980 and December 1983 in 90 homosexual men from San Francisco, Los Angeles, Houston, and New York. The median age was 37 years, with an age distribution identical to that for cases of AIDS reported to the Centers for Disease Control. Sixty-two per cent of the patients had high-grade (aggressive) subtypes of lymphoma, 29 per cent had subtypes of intermediate grade, and 7 per cent had low-grade subtypes. Histologic subtypes and malignant cell phenotypes were consistent with a B-cell origin. All but two men had extranodal lymphoma: central-nervous-system, bone-marrow, bowel, and mucocutaneous sites were most commonly involved. Thirty-five of 66 evaluable men (53 per cent) had complete responses to combination chemotherapy or radiotherapy or both, and thus far, 19 (54 per cent) of them have had a relapse. Mortality and morbidity were closely related to prodromal manifestations; death or illness have occurred in 19 (91 per cent) of the 21 men who presented with AIDS, in 26 (79 per cent) of the 33 who presented with generalized lymphadenopathy, and in 5 (42 per cent) of the 12 who had no prodromal manifestations. Mortality rates analyzed according to histologic grade were higher than currently reported rates in other patient populations. Kaposi's sarcoma or severe opportunistic infections characteristic of AIDS developed in 14 of 33 men (42 per cent) who presented with generalized lymphadenopathy and in 3 of 12 (33 per cent) without prodromal manifestations. We conclude that non-Hodgkin's lymphoma in members of an AIDS risk group is a serious manifestation of AIDS and the AIDS-related complex.

摘要

我们描述了1980年1月至1983年12月期间在旧金山、洛杉矶、休斯顿和纽约的90名同性恋男性中诊断出的非霍奇金淋巴瘤的组织学和临床特征。中位年龄为37岁,年龄分布与向疾病控制中心报告的艾滋病病例相同。62%的患者患有高级别(侵袭性)淋巴瘤亚型,29%患有中级别亚型,7%患有低级别亚型。组织学亚型和恶性细胞表型与B细胞起源一致。除两名男性外,所有男性均患有结外淋巴瘤:中枢神经系统、骨髓、肠道和皮肤黏膜部位最常受累。66名可评估男性中有35名(53%)对联合化疗或放疗或两者均有完全反应,到目前为止,其中19名(54%)复发。死亡率和发病率与前驱表现密切相关;出现艾滋病的21名男性中有19名(91%)死亡或患病,出现全身淋巴结肿大的33名男性中有26名(79%),无前驱表现的12名男性中有5名(42%)。根据组织学分级分析的死亡率高于目前其他患者群体报告的死亡率。在出现全身淋巴结肿大的33名男性中有14名(42%)以及在无前驱表现的12名男性中有3名(33%)发生了艾滋病特征性的卡波西肉瘤或严重机会性感染。我们得出结论,艾滋病风险群体成员中的非霍奇金淋巴瘤是艾滋病和艾滋病相关综合征的严重表现。

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