血管免疫母细胞性淋巴结病比较少见,我们见到一例报告如下:崔××,女,28岁,汉,已婚,山东人,工人,西宁标准件厂工作,住院号203718,1984.2.7入院。因发热,全身淋巴结先后肿大已半年,近十天高热,纳减、消瘦、多汗、淋巴结痛而入院。患者于半年前无明显诱因而发热,呈低热及中热,曾在本院门诊检查,肺有钙化灶,给以对症处理。但此后常间断发热,多在午后或夜间汗多,初颈旁及腋下淋巴结肿大,在门诊按“淋巴结核”治疗,服雷米封等抗痨,初淋巴结有缩小,热可退,但近十天呈高热,迅速出现颈、锁骨上,枕部、腋下、腹股沟等处淋巴结肿大,有疼痛、全身酸痛,汗湿 Vascular immunoblastic lymphocytic disease is relatively rare, we see a case of the report is as follows: Cui × ×, female, 28 years old, married, Shandong, workers, Xining standard factory work, hospitalization 203718, 1984.2.7 admission . Due to fever, lymph nodes have swollen the body has been six months, nearly ten days of fever, weight loss, weight loss, sweating, lymph node pain and admission. Six months ago, patients with no obvious incentive and fever, hypothermia and fever, has been in our hospital for examination, lung calcification, to symptomatic treatment. However, after the usual intermittent fever, and more in the afternoon or night sweat, paralysis and armpit lymph nodes, in the clinic by “lymph node tuberculosis” treatment, service Remy seal anti-tuberculosis, early lymph node shrinkage, heat can be retreated, but Nearly ten days was high fever, rapid neck, supraclavicular, occipital, armpit, groin and other lymph nodes, pain, body aches, sweat