Boyajian Michael K, Roussel Lauren O, Khan Galam, Stopa Edward, Bhatt Reena
Warren Alpert Medical School of Brown University, Providence, Rhode Island, United States.
Division of Plastic and Reconstructive Surgery, Brown University, Providence, Rhode Island, United States.
J Hand Microsurg. 2020 Oct;12(Suppl 1):S67-S69. doi: 10.1055/s-0039-1694288. Epub 2019 Nov 2.
Eosinophilic polymyositis is a rare disorder in which eosinophils infiltrate muscle and supporting connective tissue structures, resembling autoimmune or immunologically mediated disease. This disorder can be associated with muscle inflammation and death, and can be a cause of atraumatic compartment syndrome. This is a retrospective chart review of a case report as well as review of pertinent literature. This report presents a rare case of atraumatic compartment syndrome of the forearm caused by eosinophilic polymyositis. It provides a case summary and histological examination of this patient. This is an important case to report because it highlights eosinophilic polymyositis as a unique etiology of compartment syndrome. In appropriate clinical situations where patients do not improve despite standard interventions, one should consider the rare and unusual etiology of compartment syndrome due to eosinophilic polymyositis. Furthermore, primary surgical intervention should not be delayed while waiting to ascertain a definitive diagnosis.
嗜酸性粒细胞性多肌炎是一种罕见的疾病,其中嗜酸性粒细胞浸润肌肉和支持性结缔组织结构,类似于自身免疫性或免疫介导性疾病。这种疾病可伴有肌肉炎症和坏死,并可导致非创伤性骨筋膜室综合征。
这是一份对病例报告的回顾性图表分析以及相关文献综述。
本报告介绍了一例由嗜酸性粒细胞性多肌炎引起的前臂非创伤性骨筋膜室综合征的罕见病例。报告提供了该患者的病例总结和组织学检查结果。
报告这一病例很重要,因为它凸显了嗜酸性粒细胞性多肌炎作为骨筋膜室综合征的一种独特病因。在适当的临床情况下,若患者尽管接受了标准干预仍无改善,应考虑嗜酸性粒细胞性多肌炎导致骨筋膜室综合征这种罕见且不寻常的病因。此外,在等待明确诊断时不应延迟进行初次手术干预。