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Published online by Cambridge University Press: 26 December 2018
We present a young soldier presenting with aborted sudden cardiac death, who was found to have concomitant hypertrophic cardiomyopathy and Wolff–Parkinson–White syndrome. Along with pathological haemodynamic features of hypertrophic cardiomyopathy, an easily-inducible re-entrant tachycardia was clearly documented in our patient. Given the fatal potential of supraventricular tachycardia in hypertrophic cardiomyopathy, we postulated that his tachyarrhythmia could potentially trigger the event. Upon his refusal to receive implantable cardioverter/defibrillator therapy, we ablated anatomical arrhythmogenic substrate instead, and he remained uneventfully over 3 years on β-blocker.
Cite this article: Kim S, Song WH, Kim SS. (2018) Aborted sudden cardiac death in a young soldier with concomitant hypertrophic cardiomyopathy and Wolff–Parkinson–White syndrome. Cardiology in the Young page 252 of 255. doi: 10.1017/S1047951118002123