Objectives To discuss the clinical features, histopathologic characteristics, diagnosis and therapy of arrhythmogenic right ventricular cardiomyopathy/dysplasia.
Methods Retrospective analysis of one case of arrhythmogenic right ventricular cardiomyopathy/dysplasia clinical data and review of literatures.
Results Arrhythmogenic right ventricular cardiomyopathy/dysplasia common clinical manifestations of heart palpitations, dizziness, fainting, short breath, breath lessness, dyspnea, ECG shows delayed depolarisation epsiton wave.
Conclusions Arrhythmogenic right ventricular cardiomyopathy/dysplasia clinically rare, echocardiography and coronary CT, ECG as the main means of diagnosis, treatment to limit the movement and the drug treatment.
Key words arrhythmogenic right ventricular cardiomyopathy/dysplasia; cardiomyopathy; case reports
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