Inflammatory Myopathy with Cardiac Involvement Associated with Anti-Mitochondrial Antibodies
Baya Wafa, Ben Hassine Imen, Ben Fredj Fatma, Anoun Jihed, Mzabi Anis, Karmani Monia, Rezgui Amel, Abdessayed Nihed, Sriha Badreddine, Laouani Kechrid Chedia
Journal of Advances in Medicine and Medical Research · pp. 50–55 · Published 17 Mar 2021
10.9734/jammr/2021/v33i530845Abstract
Aim: Anti-mitochondrial antibodies (AMA) positive myositis is an atypical and rare form with various characteristics. We aim to highlight these specificities through this case report. Presentation of the Case: We present the case of a young woman diagnosed with frequent polymorphic ventricular extrasystoles and left ventricular dysfunction. Two years after, she developed asthenia and muscle weakness. Clinical and biological tests confirmed the diagnosis of myositis complicated by focal myocarditis. The immunological screening revealed negative antinuclear antibodies and positive AMA type anti-AMA-M2 and anti-M2-3E. A good clinical evolution was noted under corticosteroids and methotrexate. Discussion: Cases of primary biliary cholangitis (PBC) or positive AMA associated with other autoimmune diseases such as systemic scleroderma, Sjögren syndrome, rheumatoid arthritis and myositis have been reported. AMA’s pathogenic role on the musculoskeletal and cardiac systems remains to be clarified. Conclusion: Inflammatory myopathy associated with AMA is a rare and serious entity, characterized by a delayed diagnosis and frequent cardiac involvement, often indicating a heavy treatment.
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