
pmid: 37421929
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.
Inflammation, Necrosis, Granuloma, Muscular Diseases, Sarcoidosis, Humans, Muscle, Skeletal, Autoantibodies, Autoimmune Diseases
Inflammation, Necrosis, Granuloma, Muscular Diseases, Sarcoidosis, Humans, Muscle, Skeletal, Autoantibodies, Autoimmune Diseases
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