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Cor triatriatum dextrum

I Malcić1, L Tambić, D Richter

  • 1Department of Paediatrics, Faculty of Medicine, Zagreb, Croatia.

Insights

Cor triatriatum dextrum, a rare heart anomaly, was incidentally found in two asymptomatic children. Its long-term clinical significance, including potential arrhythmia or venous return issues, remains uncertain.

Area of Science:

  • Cardiology
  • Pediatric Cardiology
  • Congenital Heart Disease

Background:

  • Cor triatriatum dextrum is a rare congenital heart anomaly where the right atrium is divided by a membrane.
  • Historically, symptomatic cases often involve associated cardiac anomalies or persistent sinus venosus valves.
  • Echocardiography is a key diagnostic tool for identifying this condition.

Observation:

  • Two pediatric patients, a 5-year-old boy and a 9-year-old girl, presented with heart murmurs.
  • Echocardiographic evaluation revealed incidental findings of cor triatriatum dextrum in both children.
  • Both patients exhibited normal cardiac structures apart from slightly enlarged right atria and were asymptomatic.

Findings:

  • The incidental finding of asymptomatic cor triatriatum dextrum is uncommon.
  • Unlike previously reported symptomatic cases, these patients had no structural heart anomalies or persistent sinus venosus valves.
  • The right atria were mildly enlarged in both affected children.

Implications:

  • The clinical significance of asymptomatic cor triatriatum dextrum is currently conjectural.
  • Potential long-term risks may include the development of cardiac arrhythmias.
  • Further monitoring might be necessary to assess risks of impaired systemic venous return and thrombus formation.

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