皮肤粘膜淋巴结综合征(MCLS),即川畸病,是一种急性发热发疹性疾病。由川畸氏于1961年在日本首次论述后,国外和国内都陆续有不少报道,但绝大多数为儿科病例,成人发病则罕见。现将我们收治的一典型病例结合文献综述报道如下。病历摘要患者女,25岁。因发热、皮疹、关节痛20天,于1988年2月11日入院。患者元月20日起出现手 Mucosal lymph node syndrome (MCLS), that is, Kawasaki disease, is an acute febrile disease. After Kawasaki’s first discussion in Japan in 1961, many reports have been made both in foreign countries and in China, but most of them are pediatric cases, but rare in adults. Now we have a typical case of treatment combined with literature review reported below. Patient history Female, 25 years old. Due to fever, rash, arthralgia 20 days, February 11, 1988 admission. Patient appeared on hand from January 20