血管原性免疫母细胞淋巴结病(Angioimm-unoblastic lymphadenopathy 简称 AIBL),多见于中老年人,其临床特征为全身淋巴结肿大、肝脾肿大、发热、皮疹、多克隆高丙球蛋白血症等,常合并抗人球蛋白试验阳性溶血性贫血,部分病例是在病毒感染及应用某些药物后发病。本文报告1例:患者女,61岁。诉自1980年自感乏力,检查发现“脾脏肿大”,化验血红蛋白7.6g%,白细胞3,800,中性66%,淋巴34%,血小板55,000。诊断为“脾 Angioimmoblastic lymphadenopathy (AIBL), more common in the elderly, its clinical features of the generalized lymph nodes, hepatosplenomegaly, fever, rash, polyclonal hypergammaglobulinemia, etc. often Combination of anti-human globulin test positive hemolytic anemia, in some cases in the virus infection and the application of certain drugs after the onset. This article reports 1 case: patient female, 61 years old. Complaint since 1980, fatigue, inspection found that “splenomegaly”, test hemoglobin 7.6g%, 3,800 leukocytes, 66% neutral, lymphatic 34%, 55,000 platelets. Diagnosed as "spleen