Sudden cardiac death in a young athlete due to anomalous origin of both coronaries from a common ostium

Stefania Zerbo1, Giuseppe Davide Albano2, Ginevra Malta2

  • 1Section of Legal Medicine, Department of Health Promotion, Mother and Child Care, Internal Medicine and Medical Specialties, University of Palermo, Palermo, 90129, Italy. stefania.zerbo@unipa.it.

Insights

Sudden cardiac death (SCD) in young athletes is a critical public health concern. A rare congenital coronary artery anomaly combined with hypertrophic cardiomyopathy (HCM) was identified as the cause of SCD in a young athlete.

Area of Science:

  • Cardiology
  • Pathology
  • Sports Medicine

Background:

  • Sudden cardiac death (SCD) is a significant cause of mortality in young individuals, particularly athletes.
  • Congenital cardiac disorders, including cardiomyopathies and coronary anomalies, are frequently implicated in SCD.
  • Identifying underlying causes is crucial for prevention strategies.

Purpose of the Study:

  • To report a rare case of SCD in a young athlete.
  • To investigate the contributing cardiac abnormalities.
  • To emphasize the association between coronary anomalies, hypertrophic cardiomyopathy (HCM), and SCD risk.

Main Methods:

  • Case report of a 14-year-old male athlete who experienced SCD during a football game.
  • Autopsy examination to identify cardiac abnormalities.
  • Toxicological analysis to rule out substance abuse.

Main Results:

  • Autopsy revealed a congenital anomalous origin of both coronary arteries from a single aortic ostium.
  • Concomitant hypertrophic cardiomyopathy (HCM) was diagnosed.
  • Toxicology was negative for common drugs.

Conclusions:

  • The SCD was attributed to hyperkinetic ventricular arrhythmia secondary to myocardial ischemia.
  • A rare congenital coronary artery anomaly coupled with HCM poses a high risk for SCD in young athletes.
  • This case underscores the importance of recognizing these rare conditions in athletes.

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