Journal of Arrhythmia (Feb 2013)

Isolated left ventricular non-compaction cardiomyopathy associated with polymorphous ventricular tachycardia mimicking torsades de pointes

  • Oana Dickinson,
  • Marina Zakharova,
  • Barry L. Detloff,
  • Lin Y. Chen,
  • David G. Benditt,
  • Gary S. Francis,
  • Scott Sakaguchi

DOI
https://doi.org/10.1016/j.joa.2012.09.002
Journal volume & issue
Vol. 29, no. 1
pp. 43 – 46

Abstract

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Left ventricular non-compaction (LVNC) cardiomyopathy is a rare congenital disorder, classified by the American Heart Association as a primary genetic cardiomyopathy and characterized by multiple trabeculations within the left ventricle. LVNC cardiomyopathy has been associated with 3 major clinical manifestations: heart failure, atrial and ventricular arrhythmias and thromboembolic events, including stroke. In this case report, we describe a female patient with apparently isolated LVNC in whom pause-dependent polymorphic ventricular tachycardia suggesting torsades de pointes occurred in the presence of a normal QT interval.

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