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Arrhythmogenic right ventricular cardiomyopathy
  1. Roopali Soni1,
  2. Yvette Oade2
  1. 1Department of Paediatrics, Yorkshire Deanery, Leeds, UK
  2. 2Department of Paediatrics, Calderdale Royal Hospital, Halifax, UK
  1. Correspondence to Dr Roopali Soni, roopali.soni{at}gmail.com

Summary

Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a rare inherited disease of the heart muscle that causes ventricular tachyarrhythmias and sudden death in young people and athletes. It results in fibrofatty replacement of the right ventricle, and the subepicardial region of the left ventricle. It is the most common cause of sudden cardiac death in young people after hypertrophic heart disease. Diagnosis can be difficult and at present there is no cure for ARVC. Prevention of sudden death is the most important management strategy. Paediatricians need to be aware of the possibility of ARVC in adolescents and young adults presenting with palpitations, fatigue, syncope or cardiac arrest. The authors present two cases of apparently healthy teenage boys who died suddenly and unexpectedly. Postmortem examination of the myocardium was strongly suggestive of ARVC in both cases.

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  • Competing interests None.

  • Patient consent Obtained.

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