Metroka C E, Cunningham-Rundles S, Pollack M S, Sonnabend J A, Davis J M, Gordon B, Fernandez R D, Mouradian J
Ann Intern Med. 1983 Nov;99(5):585-91. doi: 10.7326/0003-4819-99-5-585.
The cases of 90 homosexual or bisexual men with generalized lymphadenopathy were studied by epidemiologic, clinical, pathologic, immunologic, and genetic methods. The patients ranged in age from 20 to 52 years and had histories of multiple sexually transmitted diseases and both recreational and prescription drug use. Histologically, their lymph nodes showed three patterns: explosive follicular hyperplasia; follicular involution with expansion of the paracortical area; and a mixed pattern of follicular hyperplasia and follicular involution in the same lymph node. The frequency of HLA-DR5 was significantly increased in these patients (p less than 0.005) compared with that in controls. All patients had impaired cell-mediated immunity. Opportunistic infections, lymphomas, or Kaposi's sarcoma subsequently developed in 15 patients who had had severe immune dysfunction for the previous 3 to 13 months. We suggest that generalized lymphadenopathy is part of the spectrum of a disorder manifested by acquired immunodeficiency, opportunistic infections, Kaposi's sarcoma, and malignant lymphomas.
采用流行病学、临床、病理、免疫和遗传学方法,对90例患有全身性淋巴结病的同性恋或双性恋男性病例进行了研究。患者年龄在20至52岁之间,有多种性传播疾病史,并有娱乐性用药和处方药使用史。组织学上,他们的淋巴结呈现三种模式:爆发性滤泡增生;滤泡退化伴副皮质区扩大;同一淋巴结中滤泡增生与滤泡退化的混合模式。与对照组相比,这些患者中HLA-DR5的频率显著增加(p小于0.005)。所有患者的细胞介导免疫均受损。在之前3至13个月有严重免疫功能障碍的15例患者中,随后发生了机会性感染、淋巴瘤或卡波西肉瘤。我们认为全身性淋巴结病是一种由获得性免疫缺陷、机会性感染、卡波西肉瘤和恶性淋巴瘤所表现的疾病谱的一部分。