[Sudden death due to commotio cordis associated to non compacted myocardium]

Analía Aquieri1, Gastón Rodríguez Granillo, Manuel Vázquez Blanco

  • 1Hospital de Clínicas José de San Martín, Universidad de Buenos Aires, Buenos Aires, Argentina.

Medicina
|December 15, 2011
PubMed

Insights

Isolated non-compacted myocardium, a rare heart condition, was diagnosed in an asymptomatic 33-year-old man after cardiac arrest from commotio cordis. This case highlights the importance of advanced imaging in diagnosing cardiac abnormalities.

Area of Science:

  • Cardiology
  • Genetics

Background:

  • Non-compacted myocardium is a rare congenital cardiomyopathy defined by prominent left ventricular trabeculations.
  • It presents with low incidence and prevalence, diagnosed via Doppler echocardiogram, MSCT, or MRI.

Observation:

  • A 33-year-old asymptomatic man experienced cardiac arrest due to commotio cordis during sports.
  • Initial Doppler echocardiogram showed no abnormalities, but subsequent imaging confirmed isolated non-compacted myocardium.

Findings:

  • The patient's cardiac arrest and ventricular flutter required electrical defibrillation.
  • Advanced imaging (DE, MSCT, RMN) post-discharge confirmed isolated non-compacted myocardium, excluding coronary artery disease.

Implications:

  • This case highlights the potential coexistence of non-compacted myocardium and commotio cordis.
  • Management included beta-blocker and antiplatelet therapy, with consideration for an automatic cardioverter-defibrillator.

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