局灶性肌炎:临床和免疫病理方面的文献综述。

Alessia Pugliese, Alba Migliorato, Adele Barbaccia, Fiammetta Biasini, Olimpia Musumeci, Antonio Toscano, Carmelo Rodolico
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引用次数: 0

摘要

目的:局灶性肌炎(FM)是一种罕见的局限性骨骼肌炎症:局灶性肌炎(FM)是一种罕见的局限性骨骼肌炎症,表现为典型的小腿局部实性肿块,预后良好。在大多数病例中,该病可自行缓解或在接受免疫抑制剂治疗后缓解,但有时也会复发或发展为全身性炎症。方法:因此,我们提供了有关 FM 组织病理学特征的最新资料,以便更好地界定这种疾病的潜在病理机制。我们对1977年7月至2023年12月期间发表的英文病例报告进行了PubMed文献检索:结果:FM和其他肌炎可能表现出相似的形态学特征。对 MMP 分子的新兴研究以及未来对微小核糖核酸(miRNA)的最终研究有助于鉴别诊断:结论:临床、实验室、神经电生理和影像学检查结果可帮助做出正确诊断。然而,肌肉活检似乎是区分 FM 和其他局部软组织肿块的唯一诊断工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Focal myositis: a literature review of clinical and immunopathological aspects.

Objectives: Focal myositis (FM) is a rare and restricted skeletal muscle inflammation, presenting as a solid mass with a typical lower leg localization and benign prognosis. In most cases the process solves spontaneously or after immunosuppressant therapy, but sometimes it recurs or progresses to a systemic inflammation. The basis of the disease are mostly unknown.

Methods: Hence, we provide an update of histopathological features of FM, in order to better define the underlying pathomechanisms of this disorder. A PubMed literature search was focused on the case reports published in English from July 1977 to December 2023.

Results: FM and other myositis may show similar morphological features. Emerging studies on MMP molecules and future eventual research on microRNAs (miRNAs) could help in differential diagnosis.

Conclusions: Clinical, laboratory, neurophysiological and imaging findings can allow a correct diagnosis. However, muscle biopsy seems to be the only diagnostic tool to differentiate among FM and other localized soft tissue masses.

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