Mitral valve prolapse can present with a rare triad of ventricular arrhythmias, stroke, and MINOCA driven by atrial cardiomyopathy and myocardial fibrosis.
This case highlights the complex arrhythmic and thromboembolic risk in mitral valve prolapse, demonstrating the value of multi-modality imaging and electrophysiological assessment to guide ICD implantation and medical therapy.
Absolute Event Rate: 0% vs 0%
Abstract Background Mitral valve prolapse (MVP) has traditionally been considered a benign condition, yet malignant ventricular arrhythmias (VAs) may occur. This case illustrates a rare overlap of complex VAs, thromboembolic stroke and myocardial infarction with non-obstructive coronary arteries (MINOCA) in a patient with MVP, underscoring the value of multi-modality imaging and electrophysiological assessment for arrhythmic risk stratification. Case Summary A 50-year-old woman with MVP was referred to our Centre for arrhythmic risk assessment after documentation of frequent premature ventricular complexes and polymorphic non-sustained ventricular tachycardia (NSVT) on Holter monitoring. Eight months earlier, she had been hospitalised for ischaemic stroke, and three days later for a MINOCA. Echocardiography showed bileaflet MVP with mild mitral regurgitation, markedly thickened leaflets and severe left atrial (LA) dilatation. Cardiac magnetic resonance revealed transmural late gadolinium enhancement (ischaemic pattern) in the mid-lateral left ventricular wall. During electrophysiological study, a rapid polymorphic NSVT was induced. Given the coexistence of structural and arrhythmic high-risk features, a primary-prevention implantable cardioverter-defibrillator (ICD) was implanted. At follow-up, ICD monitoring detected paroxysmal atrial fibrillation (AF), prompting initiation of oral anticoagulation and flecainide therapy with marked suppression of VAs. Discussion Severe LA dilatation suggested atrial cardiomyopathy favouring AF episodes, likely explaining the previous embolic events and the detection of myocardial ischaemic scar. This case highlights the complexity of risk assessment in MVP, where morphological abnormalities, atrial cardiomyopathy, and myocardial left ventricular fibrosis may coexist and synergistically amplify the arrhythmic vulnerability. A multidisciplinary clinical approach is pivotal to guide individualised clinical management and optimize outcomes.
Foschini et al. (Sat,) reported a other. Mitral valve prolapse can present with a rare triad of ventricular arrhythmias, stroke, and MINOCA driven by atrial cardiomyopathy and myocardial fibrosis.