包涵体肌炎：晚期诊断病例报告

Reumatologia clinica Pub Date : 2024-11-01 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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引用次数: 0

摘要

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。

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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Inclusion Body Myositis: A Late Diagnosis Case Report

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.

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Reumatologia clinica

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