| Literature DB >> 28878587 |
Jeffrey S Hedley, Ibhar Al Mheid, Zoubin Alikhani, Maria A Pernetz, Jonathan H Kim.
Abstract
Arrhythmogenic right ventricular cardiomyopathy, a genetically inherited disease that results in fibrofatty replacement of normal cardiac myocytes, has been associated with sudden cardiac death in athletes. Long-term participation in endurance exercise hastens the development of both the arrhythmic and structural arrhythmogenic right ventricular cardiomyopathy phenotypes. We describe the unusual case of a 34-year-old, symptomatic, female endurance athlete who had arrhythmogenic right ventricular cardiomyopathy in the presence of a structurally normal right ventricle. Clinicians should be aware of this infrequent presentation when evaluating athletic patients who have ventricular arrhythmias and normal findings on cardiac imaging studies.Entities:
Keywords: Arrhythmias, cardiac/etiology/genetics/physiopathology; PKP2 protein, human; arrhythmogenic right ventricular dysplasia/complications/diagnosis/genetics/therapy; athletes; diagnosis, differential; exercise/physiology; physical endurance/physiology; tachycardia, ventricular/etiology; treatment outcome
Mesh:
Substances:
Year: 2017 PMID: 28878587 PMCID: PMC5577959 DOI: 10.14503/THIJ-16-6025
Source DB: PubMed Journal: Tex Heart Inst J ISSN: 0730-2347