包涵体肌炎：病例报告

Inclusion Body Myositis: A Case Report.

作者信息

Kaur Komalpreet, Saliba Natalie, Kar Jitesh

机构信息

Neurology, Edward Via College of Osteopathic Medicine, Auburn, USA.

Neurology, Neurology Institute of Huntsville, Inc., Huntsville, USA.

出版信息

Cureus. 2025 Apr 1;17(4):e81581. doi: 10.7759/cureus.81581. eCollection 2025 Apr.

DOI:10.7759/cureus.81581

PMID:40322365

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12045703/

Abstract

Inclusion body myositis (IBM) is an autoimmune disease characterized by chronic inflammation and mainly muscular manifestations.This report details the case of a 71-year-old male presenting with gradual-onset muscle weakness in finger flexors and quadriceps, frequent falls, and muscle biopsy findings indicative of IBM. Due to a lack of curative treatments, the patient's management focuses on supportive care, physical therapy, and mobility aids to mitigate disease progression and reduce fall risk.

摘要

包涵体肌炎（IBM）是一种以慢性炎症为特征的自身免疫性疾病，主要表现为肌肉症状。本报告详细介绍了一名71岁男性患者的病例，该患者出现手指屈肌和股四头肌逐渐出现肌无力、频繁跌倒，肌肉活检结果提示为IBM。由于缺乏治愈性治疗方法，对该患者的管理重点在于支持性护理、物理治疗和使用助行器，以减缓疾病进展并降低跌倒风险。