血管免疫母细胞性淋巴结病是一种少见的淋巴组织增生性疾病 ,一般临床医生对本病缺乏足够认识 ,病人早期临床表现不典型 ,常被漏诊或误诊 ,1999年我院收治 1例 ,报告如下。1　病例介绍　　患者男 ,5 6岁 ,1999年 7月中旬自述突然发病 ,咽痛 ,咳嗽 ,无咳痰 ,持续发热 38～ 38.9 Angioimmunoblastic cell lymphadenopathy is a rare lymphoproliferative disease. The clinician generally lacks sufficient knowledge of this disease. The patient’s early clinical presentation is not typical, and is often missed or misdiagnosed. In 1999, 1 case was treated in our hospital. as follows. 1 Case presentation Male patient, 5-6 years old. Suddenly onset in the middle of July 1999. Suffering from sore throat, cough, no cough, persistent fever 38 to 38.9