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一名68岁女性的嗜酸性筋膜炎

Eosinophilic Fasciitis in a 68-Year-Old Female.

作者信息

Chittipolu Swetha, Kennard Jennifer L, Nahar Ludmila

机构信息

Internal Medicine, North Mississippi Health Services, Tupelo, USA.

Rheumatology, North Mississippi Health Services, Tupelo, USA.

出版信息

Cureus. 2024 Feb 9;16(2):e53908. doi: 10.7759/cureus.53908. eCollection 2024 Feb.

Abstract

Eosinophilic fasciitis (EF) is an uncommon disorder of unknown etiology and poorly understood pathogenesis. In this report, we present a case of a 68-year-old female presented with a rapidly progressing skin tightening condition in her extremities associated with eosinophilia. Four months prior, the patient's initial complaint was skin sensitivity in the legs and forearms. Over time, this led to severe skin tightening, edema, and decreased range of motion. Clinical examination showed tightening of the skin over the anterior forearms, posterior knees, and calves without sclerodactyly or Raynaud's phenomenon. Laboratory investigations showed eosinophilia, elevated antinuclear antibody titer, and negative rheumatoid factor. This presentation raised suspicion of EF, and biopsy results showed scattered lymphocytic infiltrate involving associated fibrous tissue and perivascular lymphocytic inflammation that involved vessel walls. She was treated with low-dose steroids due to her diabetes but the stiffness continued. She was started with immunomodulators methotrexate, which showed improvement in symptoms, including softening in her arm tissues.

摘要

嗜酸性筋膜炎(EF)是一种病因不明、发病机制 poorly understood 的罕见疾病。在本报告中,我们介绍了一例68岁女性患者,其四肢出现快速进展的皮肤紧绷状况,并伴有嗜酸性粒细胞增多。四个月前,患者最初的主诉是腿部和前臂皮肤敏感。随着时间的推移,这导致了严重的皮肤紧绷、水肿和活动范围减小。临床检查显示前臂前部、后膝和小腿的皮肤紧绷,但无指(趾)硬皮病或雷诺现象。实验室检查显示嗜酸性粒细胞增多、抗核抗体滴度升高和类风湿因子阴性。这种表现引起了对EF的怀疑,活检结果显示散在的淋巴细胞浸润累及相关纤维组织和涉及血管壁的血管周围淋巴细胞炎症。由于她患有糖尿病,她接受了低剂量类固醇治疗,但僵硬症状仍持续存在。她开始使用免疫调节剂甲氨蝶呤治疗,症状有所改善,包括手臂组织变软。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ed5/10924695/977f964b8b47/cureus-0016-00000053908-i01.jpg

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