Focal eosinophilic myositis involving the pronator quadratus muscle and flexor tendons in a young woman: A case report

Daniel Barona-Rommy, Carlos A. Cañas, Santiago Lopez-Garcia, Luis A. Escobar-Florez, Jorge M. Madriñan-Tascon, Fabio Bonilla-Abadía
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Abstract

Introduction

Idiopathic eosinophilic myositis (IEM) is a poorly understood inflammatory myopathy. We present the case of a patient with this condition who achieved complete symptom resolution following treatment.

Case presentation

A 26-year-old female patient presented with inflammatory changes and pain in the right forearm for 30 days. Physical examination revealed tenosynovitis of the right-hand flexors. Laboratory tests showed eosinophilia and elevated IgE levels. Magnetic resonance imaging (MRI) demonstrated findings consistent with myositis affecting the pronator quadratus muscle and deep finger flexors, along with distal forearm tenosynovitis. A biopsy revealed a lymphoplasmacytic inflammatory infiltrate with abundant eosinophils in both endomysial and perimysial locations. Treatment with deflazacort and antihistamines led to complete symptom resolution.

Conclusions

IEM is an extremely rare disease with heterogeneous clinical manifestations. We hope this case report contributes to a better understanding of this condition and serves as a foundation for future studies on IEM.
局灶性嗜酸性肌炎累及旋前方肌和屈肌腱:一例报告
特发性嗜酸性肌炎(IEM)是一种鲜为人知的炎症性肌病。我们提出的情况下,患者与这种情况下取得了完全的症状解决后治疗。病例表现:女性,26岁,右前臂炎性改变及疼痛30天。体格检查显示右屈肌腱鞘炎。实验室检查显示嗜酸性粒细胞增多和IgE水平升高。磁共振成像(MRI)显示的结果与影响旋前方肌和手指深屈肌的肌炎一致,并伴有前臂远端肌腱滑膜炎。活检显示肌内膜和膜周有淋巴浆细胞性炎症浸润伴大量嗜酸性粒细胞。地沙库特和抗组胺药治疗导致症状完全缓解。结论siem是一种极为罕见的疾病,临床表现具有异质性。我们希望这一病例报告有助于更好地了解这种情况,并为今后的研究奠定基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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