Key result
A patient with arrhythmogenic right ventricular dysplasia demonstrated clinical and electrophysiological evidence of two different and sometimes simultaneous right ventricular tachycardias.
Population
1 patient, 51-year-old woman with arrhythmogenic right ventricular dysplasia
Design
Case_report
Authors
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Hypothesis-generating for multifocal VT mechanisms in ARVD; requires validation before influencing ablation strategies.
Case Report (n=1)
This case suggests a possible new mechanism for the multiform appearances of ventricular tachycardia in ARVD via simultaneous right ventricular tachycardias.
Buja et al. (1988) conducted a case report in Arrhythmogenic right ventricular dysplasia (n=1). A patient with arrhythmogenic right ventricular dysplasia demonstrated clinical and electrophysiological evidence of two different and sometimes simultaneous right ventricular tachycardias.
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