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同性恋男性的持续性全身性淋巴结病:临床、病理及免疫学特征

Persistent generalized lymphadenopathy in homosexual men: clinical, pathological and immunologic characteristics.

作者信息

Gilmore N J, Prchal J F, Jothy S

出版信息

Can Med Assoc J. 1983 Nov 1;129(9):960-5.

Abstract

Eighteen homosexual men who had had lymphadenopathy in two or more extrainguinal sites for more than 5 months but had no evidence of other illnesses or infections were studied. All had extreme malaise, and 90% had additional symptoms (fever, night sweats, weight loss or gastrointestinal dysfunction). They were compared with 10 healthy homosexual and 10 healthy heterosexual male controls. The mean numbers of circulating T8 (suppressor) lymphocytes were increased equally in the two homosexual groups, but the mean number of T4 (helper) lymphocytes was decreased only in the group with lymphadenopathy. The response to testing for recall anergy was diminished in both homosexual groups but was significantly lower in the group with lymphadenopathy. The serum immunoglobulin and complement concentrations and the numbers of circulating B lymphocytes were normal in each group. Seven of nine lymph node biopsy specimens showed characteristic hyperplasia and confluence of follicles. Thus, idiopathic persistent, generalized lymphadenopathy in homosexual men without opportunistic infections or malignant diseases appears to be a distinct syndrome; it may also be related to the acquired immune deficiency syndrome.

摘要

对18名同性恋男性进行了研究,这些男性腹股沟外两个或更多部位出现淋巴结病超过5个月,但无其他疾病或感染迹象。所有人都极度不适,90%有其他症状(发热、盗汗、体重减轻或胃肠功能紊乱)。将他们与10名健康同性恋男性和10名健康异性恋男性对照进行比较。两个同性恋组循环T8(抑制性)淋巴细胞的平均数量均同等增加,但只有淋巴结病组的T4(辅助性)淋巴细胞平均数量减少。两个同性恋组对回忆性无反应性检测的反应均减弱,但淋巴结病组显著更低。每组血清免疫球蛋白和补体浓度以及循环B淋巴细胞数量均正常。9份淋巴结活检标本中有7份显示出特征性的滤泡增生和融合。因此,无机会性感染或恶性疾病的同性恋男性特发性持续性全身性淋巴结病似乎是一种独特的综合征;它也可能与获得性免疫缺陷综合征有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2829/1875826/b3badef1ba97/canmedaj01402-0054-a.jpg

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