我院于1982.7～1989.4共收治4例皮肤粘膜淋巴结综合征,年龄为4月～3岁,发病其初期症状体征多种多样,结合1984年日本川崎病研究班对本症之六项诊断标准,无一例能达标。如4例入院时均有高热、流涕、咳嗽、咽红,3例有腹泻、颈或/和颌下淋巴结肿大、血白细胞数增高、核左移,血培养(-),2例有黄疸、肝脾肿大、SGPT增高、血沉增快。入院 Our hospital in 1982.7 ~ 1989.4 were treated 4 cases of mucocutaneous lymph node syndrome, aged 4 months to 3 years old, the onset of its initial symptoms and signs varied, combined with the 1984 Kawasaki disease research class of the disease six diagnostic criteria, no A case can meet the standard. Four cases were admitted to the hospital with fever, runny nose, cough and throat, three cases had diarrhea, cervical or / and submandibular lymph nodes, increased leucocyte count, left nucleus and blood culture (-), and 2 cases had Jaundice, hepatosplenomegaly, SGPT increased, ESR faster. Admission