包涵体肌炎：一份晚期诊断病例报告

IF 1.3 Q4 RHEUMATOLOGY

Reumatologia Clinica Pub Date : 2024-11-01 DOI:10.1016/j.reuma.2024.07.003

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。

查看原文本刊更多论文

Miositis por cuerpos de inclusión: informe de un caso de diagnóstico tardío

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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来源期刊

Reumatologia Clinica RHEUMATOLOGY-

CiteScore

2.40

自引率

6.70%

发文量

105

审稿时长

54 days

期刊介绍： Una gran revista para cubrir eficazmente las necesidades de conocimientos en una patología de etiología, expresividad clínica y tratamiento tan amplios. Además es La Publicación Oficial de la Sociedad Española de Reumatología y del Colegio Mexicano de Reumatología y está incluida en los más prestigiosos índices de referencia en medicina.