Article Text

GW24-e3868 Arrhythmogenic right ventricular cardiomyopathy/dysplasia; A case report and review literature
  1. Zheng Li-tong,
  2. Li Jia-yue,
  3. Li De-yin,
  4. Yan Mu-yang
  1. Institute of Geriatric Cardiology, Chinese PLA General Hospital


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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