Regional ischaemic immune myopathy: unraveling a rare subtype of dermatomyopathy.

IF 0.6 Q3 MEDICINE, GENERAL & INTERNAL

BMJ Case Reports Pub Date : 2024-12-15 DOI:10.1136/bcr-2024-260865

Elvina Ingrid, Catriona McLean, Maninder Mundae, Keith Lim

引用次数: 0

Abstract

Regional ischaemic immune myopathy (RIIM) is a subtype of dermatomyopathy which has distinct histopathology features of regional muscle fibre necrosis and regeneration. This case report aims to provide an in-depth exploration of RIIM, emphasising its clinical features and the crucial role of muscle biopsy as a diagnostic investigation, as well as the potential role of immunomodulatory therapies.

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区域性缺血性免疫性肌病：揭示皮肌病的一种罕见亚型。

区域性缺血性免疫性肌病（RIIM）是皮肌病的一种亚型，具有区域性肌纤维坏死和再生的独特组织病理学特征。本病例报告旨在深入探讨 RIIM，强调其临床特征、肌肉活检作为诊断检查的关键作用以及免疫调节疗法的潜在作用。

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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来源期刊

BMJ Case Reports Medicine-Medicine (all)

CiteScore

1.40

自引率

0.00%

发文量

1588

期刊介绍： BMJ Case Reports is an important educational resource offering a high volume of cases in all disciplines so that healthcare professionals, researchers and others can easily find clinically important information on common and rare conditions. All articles are peer reviewed and copy edited before publication. BMJ Case Reports is not an edition or supplement of the BMJ.