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- W4283319589 endingPage "101764" @default.
- W4283319589 startingPage "101764" @default.
- W4283319589 abstract "Idiopathic inflammatory myopathies are a heterogeneous set of systemic inflammatory disorders primarily affecting muscle. Signs and symptoms vary greatly between and within subtypes, requiring supportive laboratory and pathologic evidence to confirm the diagnosis. Several studies are typical assessments for patients with suspected inflammatory myopathy, including muscle enzymes, autoimmune markers, imaging, and muscle biopsy. Misdiagnoses of myositis are not only related to the overlap of clinical phenotype with non-inflammatory myopathies, but also due to the limitations of diagnostic tests employed. Since many of the investigative tests are non-specific, they share features with other disorders, including muscular dystrophies, endocrine, toxic, and metabolic myopathies, and other neuromuscular or rheumatologic conditions. Recognizing the limitations of tests and understanding the shared features between inflammatory and non-inflammatory myopathies can help prevent misdiagnosing myositis with one of its several mimics." @default.
- W4283319589 created "2022-06-24" @default.
- W4283319589 creator A5051045476 @default.
- W4283319589 creator A5072466477 @default.
- W4283319589 creator A5072736652 @default.
- W4283319589 date "2022-06-01" @default.
- W4283319589 modified "2023-09-25" @default.
- W4283319589 title "Is it really myositis? Mimics and pitfalls" @default.
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