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Cor Triatriatum Dexter: A Case Report in a 70-Year-Old Male
George Hanna1, Javad Savoj1, Syed Iftikhar1
1Department of Internal Medicine, UC Riverside School of Medicine/Riverside Community Hospital, Riverside, CA 92501, USA.
Insights
Cor triatriatum dexter (CTD) is a rare congenital heart defect where a membrane divides the right atrium. This case report details a patient with CTD presenting with dyspnea and fatigue.
Area of Science:
- Cardiology
- Congenital Heart Disease
- Pediatric Cardiology
Background:
- Cor triatriatum dexter (CTD) is a rare congenital anomaly.
- It arises from the persistence of the right valve of the sinus venosus.
- A membrane forms, dividing the right atrium into two chambers.
Observation:
- The degree of atrial septation influences clinical presentation.
- Asymptomatic cases may be incidentally found during procedures or diagnostics.
- Severe cases can lead to right-sided heart failure and elevated venous pressures.
Findings:
- This report details a case of CTD in a patient experiencing dyspnea and fatigue.
- The persistent valve obstructs blood flow, impacting right heart function.
- Clinical manifestations vary significantly with the severity of the septation.
Implications:
- Understanding CTD embryology is crucial for diagnosis.
- Early diagnosis and management are key to preventing complications.
- Advances in treatment offer improved outcomes for affected individuals.
Abstract:
Cor triatriatum dexter (CTD) is a rare congenital heart disease resulting from persistence of the right valve of the sinus venosus. The persistent valve forms a membrane that divides the right atrium into a proximal and a distal chamber. This disorder exhibits varying clinical manifestations depending on the degree of partitioning or septation of the right atrium. In asymptomatic patients, the disease may be discovered during surgical procedures, diagnostic testing such as echocardiography, or hemodynamic monitoring. Severe septation abnormalities may cause right-sided heart failure and elevated central venous pressures due to obstruction of the tricuspid valve, right ventricular outflow tract, or inferior vena cava. Here we report a case of CTD in a patient presenting with symptoms of dyspnea and fatigue, followed by a short discussion of the embryology and clinical implications of this congenital disease, as well as current advances in management.
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