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白塞氏综合征是一种少见的多系统损害的炎症疾病。自从1937年Behcet描述这种口腔炎、阴部溃疡和眼病的综合征以来,已有不少有关本病的报道,唯国内儿科未见有报告。兹将我院1983年收治的1例报告于下。袁某某,女,12岁,陕西兴平县人。1982年8月起指、肘、踝关节等反复疼痛,活动受限。面部及下肢胫骨前皮肤反复出现高出皮面的花生米至核桃大小的红色皮疹,疼痛,皮疹消退后留有色素沉着。1年来口腔及舌面出现
Behcet’s syndrome is a rare, multi-system inflammatory disease. Since Behcet described this syndrome of stomatitis, pudendal ulcer and eye disease in 1937, there have been many reports about this disease, but no reports have been reported for the domestic pediatrics. I will be admitted to our hospital in 1983 1 case reported below. Yuan Moumou, female, 12 years old, Xingping County, Shaanxi Province. Since August 1982, fingers, elbows, ankles and other repeated pain, limited mobility. Facial and lower extremity tibial skin repeatedly appeared above the surface of peanuts to walnut-sized red rash, pain, rash subsided after leaving pigmentation. 1 year oral and tongue appear