TY - JOUR
T1 - Myositis Mimics
AU - Michelle, E. Harlan
AU - Mammen, Andrew L.
N1 - Funding Information:
Production of this article was supported [in part] by the Intramural Research Program of the National Institute of Arthritis and Musculoskeletal and Skin Diseases of the National Institutes of Health.
Publisher Copyright:
© 2015, Springer Science+Business Media New York (outside the USA).
PY - 2015/10/21
Y1 - 2015/10/21
N2 - Patients with autoimmune myositis typically present with muscle weakness, elevated serum levels of muscle enzymes, and abnormal muscle biopsies. However, patients with other acquired myopathies or genetic muscle diseases may have remarkably similar presentations. Making the correct diagnosis of another muscle disease can prevent these patients from being exposed to the risks of immunosuppressive medications, which benefit those with myositis, but not those with other types of muscle disease. Here, we review some of the most common acquired and inherited muscle diseases that can mimic autoimmune myositis, including inclusion body myositis, limb girdle muscular dystrophies, metabolic myopathies, mitochondrial myopathies, and endocrine myopathies. We emphasize aspects of the medical history, physical exam, laboratory evaluation, and muscle biopsy analysis that can help clinicians distinguish myositis mimics from true autoimmune myositis.
AB - Patients with autoimmune myositis typically present with muscle weakness, elevated serum levels of muscle enzymes, and abnormal muscle biopsies. However, patients with other acquired myopathies or genetic muscle diseases may have remarkably similar presentations. Making the correct diagnosis of another muscle disease can prevent these patients from being exposed to the risks of immunosuppressive medications, which benefit those with myositis, but not those with other types of muscle disease. Here, we review some of the most common acquired and inherited muscle diseases that can mimic autoimmune myositis, including inclusion body myositis, limb girdle muscular dystrophies, metabolic myopathies, mitochondrial myopathies, and endocrine myopathies. We emphasize aspects of the medical history, physical exam, laboratory evaluation, and muscle biopsy analysis that can help clinicians distinguish myositis mimics from true autoimmune myositis.
KW - Acid maltase deficiency
KW - Autoimmune myopathies
KW - Dysferlinopathy
KW - Endocrine myopathies
KW - Facioscapulohumeral muscular dystrophy
KW - Inclusion body myositis
KW - McArdle’s disease
KW - Mitochondrial myopathies
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U2 - 10.1007/s11926-015-0541-0
DO - 10.1007/s11926-015-0541-0
M3 - Review article
C2 - 26290112
AN - SCOPUS:84939613762
SN - 1523-3774
VL - 17
JO - Current Rheumatology Reports
JF - Current Rheumatology Reports
IS - 10
M1 - 63
ER -