血管免疫母细胞性淋巴腺病是一种原因不明的T细胞抑制功能减退、B细胞免疫增殖性疾病。近几年始被人们所重视。国内外已有不少报道。现将我院经病理证实3例报道如下。 例1:男36岁,1988—03—20入院,因发现颈部肿物6个月伴不规则发烧,两下肢皮肤搔痒入院。查体:体温:37.6℃,血压20/12KPa,全身皮肤干燥,皮纹明显,双下肢有多角形褐色鱼鳞屑,周边游离。两 Angioimmunoblastic lymphadenopathy is an unexplained T cell suppressive function, B cell immune proliferative disease. In recent years, people have been valued. There are many reports at home and abroad. Now my hospital confirmed by pathology reported in 3 cases as follows. Example 1: Male 36 years old, admitted to the hospital from March 1988 to March 20 due to an irregular fever with a neck mass of 6 months. Physical examination: body temperature: 37.6 ℃, blood pressure 20 / 12KPa, dry skin, dermatoglyphic obvious, double limbs polygonal brown scales, the surrounding free. Two