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血管免疫母细胞性淋巴结病(Angioi m-munoblastic Lymphadenopathy,A.I.L)是近十年来新认识的免疫功能异常的淋巴组织非肿瘤性增生性疾病。特点是急性起病,发热,皮疹,全身淋巴结肿大,肝脾肿大,多株性高免疫球蛋白血症及有特殊组织学改变。本文就有关资料作一概述。病因和发病机理一.病因:A.I.L的病因不明,有认为可能与下列因素有关: (一)药物过敏:本病约有27％患者存在
Angio-m-munoblastic Lymphadenopathy (A.I.L) is a newly recognized lymphoid non-neoplastic proliferative disease that has been newly recognized in the past decade. Characterized by acute onset, fever, rash, systemic lymphadenopathy, hepatosplenomegaly, multiple strains of high immunoglobulinuria and a special histological changes. This article gives an overview of the relevant information. Etiology and pathogenesis One etiology: A.I.L’s etiology is unknown, there may be related to the following factors: (a) drug allergy: About 27% of patients with the disease exists