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Sudden cardiac death with triple pathologies: A case report
R Razuin1,2, F Nurquin2, M N Shahidan2
1Centre for Diagnostic & Research Laboratories, Faculty of Medicine, Universiti Teknologi MARA, Selangor, Malaysia.
Insights
Sudden cardiac death in young adults can stem from rare cardiomyopathies like left ventricular noncompaction (LVNC) and arrhythmogenic right ventricular (ARVC). This case highlights co-existing conditions and acute myocardial infarction as a fatal mechanism.
Area of Science:
- Cardiology and Pathology
- Sudden Cardiac Death (SCD) in young adults
Background:
- Rare cardiomyopathies, including left ventricular noncompaction (LVNC) and arrhythmogenic right ventricular cardiomyopathy (ARVC), are implicated in sudden cardiac death (SCD) in young individuals.
- LVNC is characterized by excessive left ventricular trabeculations, while ARVC involves fibro-fatty infiltration of the right ventricular myocardium.
- Both conditions can lead to fatal arrhythmias, thromboembolic events, or heart failure.
Observation:
- A 21-year-old athletic male experienced syncope and subsequently collapsed during a futsal game, requiring resuscitation.
- Post-mortem examination revealed extensive acute myocardial infarction (AMI) affecting the left ventricle and papillary muscles.
- Pathological findings also showed features consistent with LVNC and ARVC, including myocardial thinning and fibro-fatty infiltration of the right ventricle.
Findings:
- The case presented with co-existing LVNC and ARVC, a rare occurrence.
- The primary cause of death was acute myocardial infarction (AMI), an uncommon mechanism associated with isolated LVNC or ARVC.
- Histological confirmation of AMI and massive fibro-fatty infiltration of the right ventricle was established.
Implications:
- Young, physically active individuals are not immune to sudden cardiac death, even with seemingly mild or non-specific preceding symptoms.
- The presence of co-existing cardiomyopathies can present complex diagnostic and prognostic challenges.
- This case underscores the importance of thorough investigation of cardiac symptoms in athletes, as they may indicate underlying, potentially life-threatening cardiomyopathies.
Abstract:
Sudden cardiac death in young adults may be associated with rare cardiomyopathies such as left ventricular noncompaction (LVNC) and arrhythmogenic right ventricular (ARVC) cardiomyopathies. LVNC is characterised by hypertrabeculations and deep recesses of the left ventricle. ARVC presents with thin myocardium as a result of extensive fibro-fatty infiltrations. In both conditions, death may be due to arrhythmia, thromboembolic events or heart failure. We report a case of a 21-year old athletic young man who collapsed at the futsal court right after the game. He was resuscitated but expired at the hospital after a brief admission. A week earlier, he had a similar episode of syncope and revived through cardio-pulmonary resuscitation at the site. Post mortem examination showed extensive acute myocardial infarction (AMI) involving the papillary muscles and the left ventricular wall. Features of LVNC were also observed. On top of that, the right ventricle showed patchy thin myocardium as the wall was largely comprised of fat. Histology examination confirmed the presence of AMI and massive fibro-fatty infiltrations of the right ventricle. This unfortunate young man had co-existing cardiomyopathies which is rare indeed. As he succumbed to AMI, this mechanism of death is also uncommonly associated with neither LVNC nor ARVC. In conclusion, young and physically active individuals may not be spared of sudden cardiac death. Mild and non-specific symptoms should not be taken lightly as it may be the subtle signs of cardiomyopathies.
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