Hedley Jeffrey S, Al Mheid Ibhar, Alikhani Zoubin, Pernetz Maria A, Kim Jonathan H
Tex Heart Inst J. 2017 Aug 1;44(4):290-293. doi: 10.14503/THIJ-16-6025. eCollection 2017 Aug.
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.
致心律失常性右室心肌病是一种遗传性疾病,可导致正常心肌细胞被纤维脂肪组织替代,与运动员心源性猝死有关。长期参与耐力运动可加速致心律失常性右室心肌病心律失常和结构异常表型的发展。我们描述了一例不寻常的病例,一名34岁有症状的女性耐力运动员,其右心室结构正常,但患有致心律失常性右室心肌病。临床医生在评估有室性心律失常且心脏影像学检查结果正常的运动员患者时,应意识到这种罕见的表现。