Matthews Christian, Thomas David, Monteagudo Luke, Oberstar Jennifer
Department of Family Medicine and Community Health University of Minnesota Minneapolis Minnesota USA.
Division of Rheumatic and Autoimmune Diseases University of Minnesota Minneapolis Minnesota USA.
Clin Case Rep. 2025 Mar 21;13(3):e9613. doi: 10.1002/ccr3.9613. eCollection 2025 Mar.
Eosinophilic fasciitis (EF) is a rare systemic connective tissue disease involving chronic inflammation of muscle fascia and subcutaneous tissue. While the underlying pathogenesis is poorly understood, prior publications have described classic findings to support this unusual diagnosis through clinical presentation, imaging, and histology. We report a unique case of eosinophilic fasciitis in a 24-year-old male with a predominantly asymmetric presentation and related hand involvement. Key features of the physical exam, labs and MRI imaging led to the diagnosis, and the patient improved with steroids and eventually transitioned to steroid sparing therapy. This case report highlights an unusual presentation of eosinophilic fasciitis, reviews classic diagnostic criteria and underscores a situation when it may be reasonable to avoid full thickness skin biopsy and opt for early treatment.
嗜酸性筋膜炎(EF)是一种罕见的系统性结缔组织疾病,累及肌肉筋膜和皮下组织的慢性炎症。虽然其潜在发病机制尚不清楚,但先前的出版物已描述了通过临床表现、影像学和组织学来支持这一不寻常诊断的典型发现。我们报告了一例24岁男性嗜酸性筋膜炎的独特病例,其主要表现为不对称,并累及手部。体格检查、实验室检查和MRI成像的关键特征促成了诊断,患者使用类固醇后病情改善,最终过渡到类固醇减量治疗。本病例报告突出了嗜酸性筋膜炎的一种不寻常表现,回顾了经典诊断标准,并强调了在某些情况下避免进行全层皮肤活检而选择早期治疗可能是合理的。