Granulomatous myopathy co-existent immune-mediated necrotizing myopathy: A case report

Granulomatous myopathy (GM) is a rare disease characterized by non-caseating inflammation of the skeletal muscle, with sarcoidosis as a common cause. Here, we report a case of GM co-existent immune-mediated necrotizing myopathy (IMNM) in which an anti-signal recognition particle (SRP) antibody was p...

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Veröffentlicht in:Clinical neurology and neurosurgery 2023-09, Vol.232, p.107844, Article 107844
Hauptverfasser: Yin, Chunli, Yin, Shimin, Zheng, Danfeng, Huang, Ling, Fu, Qiuzhen
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Sprache:eng
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Zusammenfassung:Granulomatous myopathy (GM) is a rare disease characterized by non-caseating inflammation of the skeletal muscle, with sarcoidosis as a common cause. Here, we report a case of GM co-existent immune-mediated necrotizing myopathy (IMNM) in which an anti-signal recognition particle (SRP) antibody was positive and a muscle biopsy showed a non-caseating granulomatous structure, along with myofiber necrosis and inflammatory cell infiltration. •Sarcoidosis is a common cause of Granulomatous myopathy.•The patient has positive anti-SRP antibody.•This is a case of granulomatous myopathy co-existent with immune-mediated necrotizing myopathy.
ISSN:0303-8467
1872-6968
1872-6968
DOI:10.1016/j.clineuro.2023.107844