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患者,男,17岁。主因持续性发烧7天于1991年3月20日入院。查体发现双眼球结膜充血,口唇干燥呈鲜红色,舌、咽部粘膜弥漫性充血,左颈部可触及一2.5cm×2.5cm肿大淋巴结,有轻压痛,手、足硬肿。以掌面明显。入院后4天出现口唇干裂,杨莓舌,手足膜状脱皮,理化检查除ESR32mm/h均为阴性。诊断为皮肤粘膜淋巴结综合征。皮肤粘膜淋巴结综合征(简称MOLS)是日本川畸富作于1967年首先报告的一种原因未明的小儿热性发疹性疾病,常见于婴幼儿,男性多于女性,目前尚未见有17岁发病的报道。我们认为本病不仅
Patient, male, 17 years old. The main cause of persistent fever 7 days in March 20, 1991 admission. Physical examination found conjunctival hyperemia in both eyes, lips dry bright red, diffuse congestion of the tongue, pharynx mucosa, the left neck can reach a 2.5cm × 2.5cm swollen lymph nodes, mild tenderness, hand, foot sclerosis. Apparent palms. Four days after admission, there were chapped lips, poplar tongue, hand and foot film peeling, physical and chemical examination except ESR32mm / h were negative. Diagnosis of mucocutaneous lymph node syndrome. Mucosal lymph node syndrome (MOLS) is the first reported in 1967 by Chuan-Kuo-Fu in an unknown cause of infantile fever rash disease, common in infants and young children, more than men and women, has not yet seen 17-year-old The incidence of the report. We think this disease is not only