Cardiac involvement in a case of juvenile dermatomyositis with positive anti-melanoma differentiation associated protein 5 antibody.
Melike Mehveş KaplanElif ÇelikelVildan GüngörerZahide Ekinci TekinHazım Alper GursuSanem Eryılmaz PolatGuzin CinelBanu Çelikel AcarPublished in: International journal of rheumatic diseases (2023)
Juvenile dermatomyositis (JDM) is an autoimmune disease characterized by muscle weakness and specific skin lesions, as well as non-muscular involvement such as interstitial lung disease (ILD), cardiac involvement and arthritis. Anti-melanoma differentiation-associated protein 5 (anti-MDA5)-positive JDM patients are typically characterized by the presence of skin ulcers and rapidly progressing ILD (RP-ILD). Although cardiac involvement is not an expected involvement in anti-MDA5-positive JDM cases, it is significant because it can be fatal. In this report, an anti-MDA5 myositis-specific autoantibody-positive JDM case referred with the diagnosis of psoriatic arthritis in whom cardiomyopathy and arrhythmia were detected in follow-up is presented. Since cardiac involvement is associated with mortality, it would be useful to follow up anti-MDA5 positive patients for cardiac involvement in addition to lung involvement. Tofacitinib is a promising treatment option in treatment-resistant JDM.
Keyphrases
- interstitial lung disease
- systemic sclerosis
- rheumatoid arthritis
- end stage renal disease
- left ventricular
- idiopathic pulmonary fibrosis
- ejection fraction
- newly diagnosed
- chronic kidney disease
- breast cancer cells
- heart failure
- prognostic factors
- multiple sclerosis
- peritoneal dialysis
- skeletal muscle
- risk factors
- wound healing
- smoking cessation
- cell death
- skin cancer
- replacement therapy
- basal cell carcinoma