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血管免疫母细胞性淋巴结病(AIL),又称血管免疫母细胞性淋巴结病伴异常蛋白症(AILD)。现将最近我们遇到的1例报告如下。患者男,61岁,于1982年11月9日因长期发热、全身淋巴结肿大2年余伴腹疼腹泻1周入院。查体:T38.5℃,P108次/分,BP120/80mmHg,皮肤粘膜无黄染,无皮疹及出血点,左颈部可触及枣子大淋巴结2个,表面光滑,
Angioimmunoblastic lymphadenopathy (AIL), also known as angioimmunoblastic lymphadenopathy with abnormal protein disease (AILD). Now we have encountered a recent report as follows. Male patient, 61 years old, on November 9, 1982 due to long-term fever, systemic lymphadenopathy more than 2 years with abdominal pain and diarrhea 1 week hospitalization. Physical examination: T38.5 ℃, P108 times / min, BP120 / 80mmHg, skin and mucosa no yellow dye, no rash and bleeding points, the left neck can reach jujube large lymph nodes 2, the surface is smooth,