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同性恋男性持续性全身性淋巴结病的纵向研究:与获得性免疫缺陷综合征的关系。

Longitudinal study of persistent generalised lymphadenopathy in homosexual men: relation to acquired immunodeficiency syndrome.

作者信息

Mathur-Wagh U, Enlow R W, Spigland I, Winchester R J, Sacks H S, Rorat E, Yancovitz S R, Klein M J, William D C, Mildvan D

出版信息

Lancet. 1984 May 12;1(8385):1033-8. doi: 10.1016/s0140-6736(84)91449-1.

Abstract

42 homosexual or bisexual men with persistent generalised lymphadenopathy not attributable to an identifiable cause have been followed longitudinally since February, 1981. Lymphadenopathy was accompanied by fatigue, low-grade fever and/or night sweats (57%), splenomegaly (29%), leucopenia (40%), hypergamma - globulinaemia (76%), and diminished proportion and absolute numbers of helper T cells (95%). Of the 26 patients who had lymph node biopsy, all showed benign reactive hyperplasia. After 15-30 (median 22) months, 8 patients have met criteria for the diagnosis of acquired immunodeficiency syndrome (AIDS). This outcome was associated with previous heavy nitrite inhalant use, with the presence of night sweats, with leucopenia, and with the triad of constitutional symptoms, splenomegaly, and leucopenia. In addition, a lower mean absolute helper T cell count and an increased frequency of anergy to mumps intradermal antigen and of herpes simplex virus isolation distinguished these patients from those remaining in the cohort, who seem to be stable and in some cases to have improved.

摘要

自1981年2月以来,对42例患有持续性全身性淋巴结病且无明确病因的同性恋或双性恋男性进行了纵向随访。淋巴结病伴有疲劳、低热和/或盗汗(57%)、脾肿大(29%)、白细胞减少(40%)、高丙种球蛋白血症(76%)以及辅助性T细胞比例和绝对数量减少(95%)。在26例行淋巴结活检的患者中,均显示为良性反应性增生。15至30个月(中位数22个月)后,8例患者符合获得性免疫缺陷综合征(AIDS)的诊断标准。这一结果与既往大量吸入亚硝酸盐、盗汗、白细胞减少以及体质症状、脾肿大和白细胞减少三联征有关。此外,较低的平均辅助性T细胞绝对计数以及对腮腺炎皮内抗原无反应和单纯疱疹病毒分离频率增加,使这些患者与队列中其余患者区分开来,其余患者似乎病情稳定,有些病例甚至有所改善。

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