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Three's a Crowd - An Extremely Rare Case of Cor Triatriatum Dexter
Insights
Cor triatriatum dextrum, a rare congenital heart anomaly, involves atrial division. This case highlights its association with other cardiac defects, often diagnosed in adulthood.
Area of Science:
- Cardiology
- Congenital Heart Disease
- Cardiac Anatomy
Background:
- Cor triatriatum is a rare congenital cardiac anomaly causing atrial division, resulting in a tri-atrial heart.
- Cor triatriatum dextrum presents with varied clinical signs and potential associated anomalies.
- Understanding this rare disorder contributes to clinical knowledge.
Purpose of the Study:
- To report a case of cor triatriatum dextrum.
- To highlight associated congenital cardiac anomalies.
- To contribute to the understanding of this rare condition.
Main Methods:
- Case report of a 40-year-old man with palpitations, edema, and heart failure.
- Diagnostic evaluations included 2D echocardiography, transesophageal echocardiography (TEE), and cardiac catheterization.
- Conservative management was initiated, with referral for surgical evaluation.
Main Results:
- The patient presented with atrial fibrillation, heart failure, and severe right atrial enlargement.
- Diagnostic imaging revealed a septated right atrium, possible unroofed coronary sinus, patent foramen ovale (PFO), and a coronary-cameral fistula.
- Clinical improvement was achieved with medical management.
Conclusions:
- Cor triatriatum dextrum is extremely rare, with prevalence <0.01% in high-volume labs.
- This case underscores the association of cor triatriatum dextrum with persistent left superior vena cava, unroofed coronary sinus, PFO, and left-to-right shunt.
- Unlike left-sided cor triatriatum, right-sided forms may be diagnosed in adulthood due to lack of pulmonary involvement.
Introduction:
Cor triatriatum is a congenital cardiac anomaly in which the left (sinister) or right (dexter) atrium is divided into two compartments by residual embryonic tissue, resulting in a tri-atrial heart. As cor triatriatum dextrum can present clinically in various ways and have multiple associated cardiac anomalies, this report attempts to contribute to what is known about this exceedingly rare disorder.
Case:
A 40 year old Hispanic man with a medical history of gastritis presented with complaints of palpitations, dizziness and bilateral lower extremity edema. He was found to have atrial fibrillation and new onset heart failure. The patient was admitted for rate control and further evaluation, which revealed several cardiac anomalies. Initial 2D echocardiography demonstrated severe right atrial enlargement, right ventricular hypertrophy and an engorged coronary sinus, which prompted further assessment of the patient's cardiovascular anatomy. Transesophageal echocardiography (TEE) revealed a severely enlarged, septated right atrium with a possible unroofed coronary sinus and a small patent foramen ovale (PFO). Left- and right-heart catheterization established a coronary-cameral fistula between the right coronary artery (RCA) and right atrium, as well as left-to-right shunt. The patient improved clinically with conservative management including diet modification, furosemide and digoxin for fluid and rate control, and was referred to cardiothoracic surgery for further evaluation.
Discussion:
Cor triatriatum dextrum is an extremely rare cardiac condition: In high-volume echocardiographic laboratories, prevalence is less than 0.01 percent. This case highlights the association between cor triatriatum and other congenital cardiac anomalies, including persistent left superior vena cava with an unroofed coronary sinus, PFO and left-to-right shunt; all of which were found in this patient. While cases of cor-triatriatum sinistrum often require correction in infancy (due to left sided heart failure, pulmonary edema and cyanosis), cor-triatriatum dextrum is sometimes diagnosed in adulthood due to the lack of left heart and pulmonary involvement.
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