血管性原始免疫细胞性淋巴腺病三例报告及文献复习

报道３例血管性原始免疫细胞性淋巴腺病，并收集１９７８至１９９４年３月间国内报道的２１８例资料，共２２１例进行综合分析，４０岁以上者居多，儿童占１６．５％，临床主要表现为淋巴结肿大，发热，肝脾肿大，皮疹，血沉快和多克隆克疫球蛋白血症，淋巴结活检特性为三联征，是确诊的主要论据，治疗首选择肾上腺皮质激素。

Angio-Immunoblastic Lymphadenopathy Report of 3 Cases and Review of Literature

cases of Angio-immunoblastic lymphadenopathy were reported, and another 218 cases were collected from the reports of Chinese literature from 1978 to Mar. 1994, so that a total number of 221 cases were analyzed. Majority of the cases reported were more than 40 years old and 16.5 percent were children. Main manifestation of the clinical symptoms were enlargement of lymph nodes, fever, hepatosplenomegaly, skin rash, rapid red cell sedimentation rate and polyclonal hyperglobulinemia. The characteristic of lymph nodes biopsy are three union syndrome', which is the main diagnosis. Adrenocortial hormones is the first choice of treatment.