The natural history of arrhythmogenic right ventricular cardiomyopathy

Am Heart Hosp J. 2007 Fall;5(4):259-62. doi: 10.1111/j.1541-9215.2007.06521.x.

Abstract

The authors describe the case of a 66-year-old woman with arrhythmogenic right ventricular dysplasia masqueraded as dilated cardiomyopathy. Her medical history included recurrent episodes of syncope beginning at the age of 28. The natural history of the disease is discussed.

Publication types

  • Case Reports

MeSH terms

  • Aged
  • Bundle-Branch Block / pathology*
  • Cardiomyopathies / pathology*
  • Catheter Ablation
  • Dyspnea
  • Female
  • Heart Ventricles / pathology*
  • Humans
  • Procainamide / therapeutic use
  • Tachycardia, Ventricular / diagnosis
  • Tachycardia, Ventricular / drug therapy
  • Tachycardia, Ventricular / pathology*

Substances

  • Procainamide