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我院曾发现二例血管免疫母细胞性淋巴结病(AILD),现报告如下。例1 女患,71岁。1987年3月无明显诱因出现发冷发热(T39.8℃)。起病后3天躯干、四肢出现斑丘疹伴搔痒.经用青霉素、洁霉素等治疗20余天,体温渐转正常,皮疹消退.同年7月和10月各有一次类似发病,抗生素治疗无效,用激素退热效果明显.入院检查:T38.1℃,Bp14.6/9.3kPa(110/10mmHg)。胸背部可见散在的斑丘疹,压之退色,双颌下和双腋下可触及数个黄豆大小的淋巴
Our hospital has found two cases of angioimmunoblastic lymphadenopathy (AILD), are as follows. Example 1 female patient, 71 years old. March 1987 no obvious incentive to chilling fever (T39.8 ℃). 3 days after onset of torso, rash and pruritus appeared limbs with penicillin, lincomycin and other treatment for more than 20 days, body temperature gradually turned normal, the rash subsided in July the same year and October each with a similar incidence of antibiotic therapy ineffective, Hormone withdrawal effect with hormone obviously. Admission examination: T38.1 ℃, Bp14.6 / 9.3kPa (110 / 10mmHg). Chest and back visible scattered rash, pressure of the fade, double submandibular and double underarms can reach several soybean-sized lymph nodes