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 |
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Format: | Artikel |
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. |
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ISSN: | 0303-8467 1872-6968 1872-6968 |
DOI: | 10.1016/j.clineuro.2023.107844 |