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继 Shulman 之后,Rodnan 等采用了嗜酸性细胞增多性筋膜炎的这个名称。其他报告中采用Shulman 综合征、弥漫性嗜酸性细胞增多症性筋膜炎、弥漫性筋膜炎等。本病的临床表现主要有硬皮病样的皮肤病变,血沉快,高γ球蛋白血症,周围血中嗜酸性细胞增多等。自1974年 Shulman 报告后,在欧美计有35例,日本也有数例记载。发病以秋冬为多,迅速发病,逐渐发现身体异常,在定型的病例,有低烧、全身无力、肌痛等,相
Following Shulman, Rodnan et al. Used the name eosinophilic fasciitis. Other reports used Shulman syndrome, diffuse eosinophilic fasciitis, diffuse fasciitis and so on. The clinical manifestations of the disease are mainly scleroderma-like skin lesions, ESR, high-gamma globulin, peripheral blood eosinophilia and so on. Since Shulman’s report in 1974, there are 35 cases in Europe and the United States, and there are several cases in Japan. The incidence of autumn and winter as much, rapid onset, and gradually found abnormalities in the stereotyped cases, with low-grade fever, generalized weakness, myalgia, etc.