血管免疫母细胞性淋巴结病一例报告

<正> 本文报道一例血管免疫母细胞淋巴结病,也有称为“免疫母细胞淋巴结病”等。此病是近年来才认识到的一种可能与自身免疫有关的非肿瘤性B淋巴细胞过度增生所致的高免疫反应状态疾病。其发病机理未明,相当一部分人与过敏因素有关。临床上本病多见于50岁以上老年人。以发热、全身不适、消瘦、盗汗及皮肤搔痒为主要症状;部分病人伴有关节痛,全部病人均有浅部淋巴结普遍增大,一般直径不大于3、4厘米。皮疹、肝脾肿大十分常见。实验室检查呈正

ANGIOIMMUNOBIASTIC LYMPHADENOPATHY (ASLD)

This article reports a clinically seldom seen case of AILD. Only in recent years has this disease been recognized. It is a disorder related not to tumor, but to high immunoreaction, and probably to B-lymphocytosis. It shows a specific clinical as well as pathologic picture. Since Lukes first presented his discovery of the disorder in a report in 1975, it has been reported in a few articles in our country. Because the diagnosis, treatment and prognosis of the disease differ from those of malignant tumor and Hodkin's disease, the auther has made this report to bring it to clinician's and pathologist's attention.