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Necrotizing myopathy presenting as congestive heart failure and life-threatening ventricular arrhythmias: a case report.

Authors :
Lim, Kyunghee
Park, Jong Sung
Yoon, Byeol-A
Han, Song-Hee
Source :
European Heart Journal Case Reports; Jun2021, Vol. 5 Issue 6, p1-8, 8p
Publication Year :
2021

Abstract

Background Necrotizing autoimmune myopathy is a rare subtype of idiopathic inflammatory myopathy; however, it can be associated with fatal cardiac manifestations. Case summary A 58-year-old female patient was referred for congestive heart failure with dysrhythmia. Electrocardiograms showed ventricular arrhythmias of various QRS complex morphologies and coupling intervals with beat-to-beat differences. Despite optimal medical therapy for heart failure, the patient was admitted for the progression of dyspnoea and generalized motor weakness. The burden of non-sustained ventricular tachycardia gradually increased, and ventricular fibrillation eventually occurred. In view of a differential diagnosis of an inflammatory myocardial diseases such as sarcoidosis, a cardiac biopsy was performed. However, pathologic examinations revealed only necrotic muscle fibres without granuloma. Further examinations revealed proximal dominant motor weakness, an elevated serum creatinine-phosphokinase level, myogenic potentials on needle electromyography, and biceps muscle biopsy findings that were compatible with necrotizing autoimmune myopathy. High-dose steroid therapy improved the patient's motor weakness, including her respiratory impairment, and successfully suppressed ventricular arrhythmias. Discussion This case suggests that intensive immunosuppressive therapy with high-dose steroid could be useful in the necrotizing autoimmune myopathy manifested as congestive heart failure and life-threatening ventricular arrhythmias. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
25142119
Volume :
5
Issue :
6
Database :
Complementary Index
Journal :
European Heart Journal Case Reports
Publication Type :
Academic Journal
Accession number :
151310448
Full Text :
https://doi.org/10.1093/ehjcr/ytab075