Inclusion Body Myositis: A Late Diagnosis Case Report.

Reumatologia clinica Pub Date : 2024-11-01 Epub Date: 2024-10-28 DOI:10.1016/j.reumae.2024.10.002
Deysi Andrea Hernández-Rivero, Lisette Bazán-Rodríguez, María Del Pilar Cruz-Domínguez, Gabriela Medina, Ana Lilia Peralta Amaro, Olga Vera-Lastra
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Abstract

Inclusion body myositis is a idiopathic inflammatory myopathy characterized by muscle weakness and dysphagia, with muscle biopsy showing inflammation and rimmed vacuoles. We present the case of a patient who was diagnosed with polymyositis but due to lack of response to treatment, a new biopsy revealed inclusion body myositis.

包涵体肌炎:晚期诊断病例报告
包涵体肌炎是一种特发性炎症性肌病,以肌无力和吞咽困难为特征,肌肉活检显示炎症和边缘空泡。我们介绍了一例患者的病例,该患者曾被诊断为多发性肌炎,但由于对治疗缺乏反应,新的活组织检查发现了包涵体肌炎。
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