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急性发热性皮肤粘膜淋巴结综合征(MLNS)是一种原因不明的发热性出疹性疾病。自1967年首先由日本川崎报导后,世界各地陆续有所发现。近年来我国北部地区也相继报导。中华儿科杂志1979年第2期发表了详细的资料。但在我国的南部地区仍较少见。1979年夏季期间我们收治了2例病孩,与日本MLNS研究委员会1974年第2次修订的MLNS的诊断要点有很多支持的地方,故诊为MLNS。现报导如下,供同志们参考。例1 男,8月,住院号16066。因持续发热7天,颈淋巴结肿大5天,皮疹3天入院。入院前5天曾在我院门诊按上炎治疗,曾用青、链霉素等抗菌素治疗,仍发热至40℃,咳嗽。入院前3天发现患儿双大腿内侧、颈、背部有环形红斑,压之退色,日渐增
Acute febrile mucocutaneous lymph node syndrome (MLNS) is an unexplained febrile illness. Since the first report by Kawasaki in 1967 in Japan, it has been discovered in various parts of the world. In recent years, northern China has also been reported. Chinese Journal of Pediatrics No. 2, 1979 published detailed information. However, it is still rare in the southern part of our country. During the summer of 1979, we treated 2 patients and gave a lot of support for the diagnosis of MLNS, which was revised by Japan’s MLNS Research Council in 1974 for the second time. Therefore, the diagnosis is MLNS. Now reported as follows, for comrades reference. Example 1 male, August, hospital number 16066. 7 days due to persistent fever, cervical lymph node enlargement 5 days, rash 3 days admission. 5 days before admission in our hospital clinically treated by inflammation, had green, streptomycin and other antibiotics, still fever to 40 ℃, cough. 3 days before admission found that children with double thigh inside, neck, back with annular erythema, pressure fade, increasing day by day