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我院于1991～1996年间共收治8例皮肤粘膜淋巴结综合征,年龄为2～5岁。其发病初期症状体征多种多样,结合1984年日本川畸病研究班对本症的六项诊断标准,无一例能达标。如8例入院时均有高热、咽红,6例有颈部淋巴结肿大、腹痛、腹胀及腹泻。2例仅表现高热及手掌足底皮肤潮红、手足及指(趾)端呈坚实性肿胀。血白细胞数增高,血沉增快,血小板数减少。入院时诊断拟急性淋巴结炎,上感,药物性皮疹等。病程中皮疹6例在第2～3日出现;皮疹特点为全身散在红色斑丘疹或猩红
In our hospital from 1991 to 1996 were treated 8 cases of mucocutaneous lymph node syndrome, aged 2 to 5 years old. The onset of symptoms and signs of a variety of early, combined with the 1984 Sichuan Institute of Kawasaki disease of the six diagnostic criteria, no one can meet the standard. Such as 8 cases were admitted to high fever, throat, 6 cases of cervical lymph node enlargement, abdominal pain, abdominal distension and diarrhea. 2 cases showed only high fever and palms and soles of the skin flushing, hands and feet and finger (toe) end was solid swelling. Increased number of white blood cells, erythrocyte sedimentation rate, reduced platelet count. When admitted to the hospital to diagnose acute lymphocytic inflammation, on the flu, drug-induced rash. Rash in the course of 6 cases occurred in the first 2 to 3; rash characterized by systemic scattered red rash or scarlet