Ge Gai, Su Fei, Chen Hui, Hu Bin, Chen Jinbo
Department of Dermatology, Traditional Chinese and Western Medicine Hospital of Wuhan, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, People's Republic of China.
Department of Dermatology, Wuhan No. 1 Hospital, Wuhan, People's Republic of China.
Clin Cosmet Investig Dermatol. 2025 May 19;18:1219-1223. doi: 10.2147/CCID.S518593. eCollection 2025.
Eosinophilic fasciitis (EF) is a rare sclerodermic form disease characterized by upper and lower limb edema. Here, we present a rare recurrent EF. A 57-year-old man presented to dermatology outpatient with skin induration on his both limbs. A diagnose of EF was made 12 years ago. According to swelling induration, eosinophilia >0.5 × 10/l, hyperintense fascia on MRI T2-weighted images, and fascial thickening with accumulation of lymphocytes and macrophages with eosinophilic infiltration, he was diagnosed as EF. Patient was successfully treated with oral prednisone and methotrexate (MTX). To our knowledge, this is the first report of recurrent EF during the last twenty years. We report this case to analyze the reasons for recurrent EF and review-related literature to further provide experience for the diagnosis and treatment of recurrent EF.
嗜酸性筋膜炎(EF)是一种罕见的硬皮病样疾病,其特征为上下肢水肿。在此,我们报告一例罕见的复发性EF。一名57岁男性因双下肢皮肤硬结就诊于皮肤科门诊。12年前被诊断为EF。根据肿胀硬结、嗜酸性粒细胞增多>0.5×10⁹/L、MRI T2加权像上筋膜高信号以及筋膜增厚伴淋巴细胞和巨噬细胞聚集及嗜酸性粒细胞浸润,他被诊断为EF。患者口服泼尼松和甲氨蝶呤(MTX)治疗成功。据我们所知,这是过去二十年来复发性EF的首例报告。我们报告此病例以分析复发性EF的原因并复习相关文献,以便为复发性EF的诊断和治疗进一步提供经验。