Key result
A 20-year-old male with ventricular non-compaction died of acute ventricular arrhythmia, highlighting the risk of sudden cardiac death in this rare cardiomyopathy.
Case Report (n=1)
Ventricular non-compaction is a rare cardiomyopathy that can lead to fatal ventricular arrhythmias and sudden cardiac death, underscoring the critical need for early diagnosis and appropriate management.
Alerts clinicians to SCD risk in ventricular non-compaction; leaves open optimal risk stratification and prevention strategies.
<ns3:p>Ventricular non-compaction (VNC) is a rare myocardium disorder, which can be both genetic and sporadic. A poor wall compaction process or an excessive trabeculae formation may be at the genesis of myocardial hypertrabeculation with multiple recesses. It is often complicated by ventricular dysfunction, arrhythmias and cardiac embolism. Herein we report a case of a 20-year-old male patient with no particular past medical history who was followed up at the cardiology department for dyspnea. Echocardiography showed reduced ejection fraction of the left ventricle with potential hypertrabeculation in the right ventricle, confirmed by cardiac MRI. The patient was not put under medication and was later lost to follow-up. He died few months later without a clear cause explaining death. A forensic autopsy was performed that attributed death to acute ventricle arrhythmia secondary to VNC, emphasizing the major role of an early and specific treatment to avoid such a fatal outcome.</ns3:p>
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Mannoubi et al. (2020) conducted a case report in Ventricular myocardial non-compaction (n=1). Ventricular non-compaction was evaluated on Sudden cardiac death. A 20-year-old male with ventricular non-compaction died of acute ventricular arrhythmia, highlighting the risk of sudden cardiac death in this rare cardiomyopathy.
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