Volume 2010, Issue 1 383852
Case Report
Open Access

Myotonic Dystrophy Initially Presenting as Tachycardiomyopathy Successful Catheter Ablation of Atrial Flutter

S. Asbach

S. Asbach

II. Medizinische Klinik, Klinikum Coburg, 96450 Coburg, Germany klinikum-coburg.de

Medizinische Universitätsklinik, Innere Medizin III, Abt. für Kardiologie und Angiologie, 79106 Freiburg, Germany uniklinik-freiburg.de

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K. J. Gutleben

K. J. Gutleben

II. Medizinische Klinik, Klinikum Coburg, 96450 Coburg, Germany klinikum-coburg.de

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P. Dahlem

P. Dahlem

Klinik für Kinder und Jugendliche, Klinikum Coburg, 96450 Coburg, Germany klinikum-coburg.de

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J. Brachmann

J. Brachmann

II. Medizinische Klinik, Klinikum Coburg, 96450 Coburg, Germany klinikum-coburg.de

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G. Nölker

Corresponding Author

G. Nölker

II. Medizinische Klinik, Klinikum Coburg, 96450 Coburg, Germany klinikum-coburg.de

Herz- und Diabeteszentrum Nordrhein-Westfalen, 11 Georgstraße, 32545 Bad Oeynhausen, Germany hdz-nrw.de

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First published: 24 August 2010
Academic Editor: Debabrata P. Mukherjee

Abstract

Myotonic dystrophy is a genetic muscular disease that is frequently associated with cardiac arrhythmias. Bradyarrhythmias, such as sinus bradycardia and atrioventricular block, are more common than tachyarrhythmias. Rarely, previously undiagnosed patients with myotonic dystrophy initially present with a tachyarrhythmia. We describe the case of a 14-year-old boy, who was admitted to the hospital with clinical signs and symptoms of decompensated heart failure and severely reduced left ventricular function. Electrocardiography showed common-type atrial flutter with 2 : 1 conduction resulting in a heart rate of 160 bpm. Initiation of medical therapy for heart failure as well as electrical cardioversion led to a marked clinical improvement. Catheter ablation of atrial flutter was performed to prevent future cardiac decompensations and to prevent development of tachymyopathy. Left ventricular function normalized during followup. Genetic analysis confirmed the clinical suspicion of myotonic dystrophy as known in other family members in this case.

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