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血管免疫母细胞性淋巴结病(Angioimmu-noblastie Lymphadenopathy,)根据其临床及病理学特点又命名为血管免疫母细胞性淋巴结病伴异常蛋白血症(Angioimmunoblastic Lymphad-enopathy with Dysproteinemia简称AILD),是一种少见的、免疫功能异常的淋巴组织增生性疾病,国内报道尚少,我院曾收治三例现报告如下: 临床资料例1,男,53岁。以发热10余天颈部肿物6～7天于1986年1月11日入院。T39℃,周身淋巴结肿大,肝脾大。Hb130g/L,WBC40×10~9/L,免疫球蛋白正常,蛋白电泳α_20.139,余正常。X
Vascular cell immune mother lymphadenopathy (Angioimmu-noblastie Lymphadenopathy,) according to their clinical and pathological features and named immunoblastic lymphadenopathy associated with abnormal vascular albumin (Angioimmunoblastic Lymphadenopathy with Dysproteinemia referred AILD), a Rare, immune dysfunction of lymphoproliferative diseases, domestic reports are still less, our hospital has admitted three cases are as follows: Clinical data example 1, male, 53 years old. To fever more than 10 days neck mass 6 to 7 days in January 11, 1986 admission. T39 ℃, lymphadenopathy, hepatosplenomegaly. Hb130g / L, WBC40 × 10 ~ 9 / L, normal immunoglobulin, protein electrophoresis α_20.139, more than normal. X.