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同性恋男性的持续性弥漫性淋巴结病:终点还是前驱症状?

Persistent diffuse lymphadenopathy in homosexual men: endpoint or prodrome?

作者信息

Abrams D I, Lewis B J, Beckstead J H, Casavant C A, Drew W L

出版信息

Ann Intern Med. 1984 Jun;100(6):801-8. doi: 10.7326/0003-4819-100-6-801.

Abstract

Seventy homosexual men with unexplained persistent diffuse lymphadenopathy enrolled in a prospective natural history study from November 1981 to November 1982. These men had demographic, clinical, and laboratory findings similar to those of homosexual patients with the acquired immunodeficiency syndrome. Pathologic examination of lymph node biopsies from 35 patients showed florid follicular hyperplasia. Despite benign reactive pathologic findings, most patients had constitutional symptoms and recurrent non-life-threatening infections. All had evidence of immune dysfunction with B-lymphocyte activation and inversion of the T-lymphocyte helper: suppressor ratio. To date, none of our patients has developed the more malignant manifestations of the acquired immunodeficiency syndrome. The lymphadenopathy syndrome may be an alternative phenotypic response to the "acquired immunodeficiency syndrome agent."

摘要

1981年11月至1982年11月,70名患有不明原因持续性弥漫性淋巴结病的同性恋男性参加了一项前瞻性自然史研究。这些男性的人口统计学、临床和实验室检查结果与获得性免疫缺陷综合征的同性恋患者相似。对35例患者的淋巴结活检进行病理检查,结果显示为明显的滤泡增生。尽管病理检查结果为良性反应,但大多数患者有全身症状和反复出现的非危及生命的感染。所有患者均有免疫功能障碍的证据,表现为B淋巴细胞活化和T淋巴细胞辅助细胞与抑制细胞比例倒置。迄今为止,我们的患者中没有一人出现获得性免疫缺陷综合征更恶性的表现。淋巴结病综合征可能是对“获得性免疫缺陷综合征病原体”的另一种表型反应。

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