Related Experiment Video
Updated: Jun 4, 2026

Echocardiographic Evaluation of Atrial Communications before Transcatheter Closure
Published on: February 8, 2022
Echocardiographic diagnosis of divided right atrium-cor triatriatum dextrum
Ramush Bejiqi1, Ragip Retkoceri, Hana Bejiqi
1Pediatric Clinic, University Clinical Centre of Kosova, Prishtina, Kosova.
Insights
Cor triatriatum dextrum, a rare congenital heart anomaly, involves right atrial division. This case highlights a unique instance associated with atrial septal defect and pulmonary stenosis.
Area of Science:
- Cardiology
- Congenital Heart Disease
- Cardiac Anatomy
Background:
- Cor triatriatum is a congenital anomaly where an atrium is divided by a membrane.
- Cor triatriatum sinistrum (left atrial division) is clinically recognized, while cor triatriatum dextrum (right atrial division) is rare and primarily a pathological finding.
- The right atrial partition is typically associated with variations in the Eustachian and Thebesian valves.
Observation:
- This report details a rare case of cor triatriatum dextrum.
- The dividing partition in the right atrium was situated between the systemic venous sinus and the distal right atrium, attaching to the inferior vena cava orifice.
- The patient presented with a large atrial septal defect and valvular pulmonary stenosis.
Findings:
- A case of divided right atrium (cor triatriatum dextrum) is described.
- The anomaly was associated with significant comorbidities: a large atrial septal defect and valvular pulmonary stenosis.
- This presentation underscores the rare but complex nature of right atrial partitioning.
Implications:
- Understanding rare congenital anomalies like cor triatriatum dextrum is crucial for accurate diagnosis and surgical planning.
- The association with other cardiac defects necessitates comprehensive echocardiographic and potentially intraoperative assessment.
- Further case reports can enhance the understanding of the spectrum and clinical significance of right atrial division.
Abstract:
First reported in 1868, cor triatriatum, that is, a heart with 3 atria (triatrial heart), is a congenital anomaly in which the left atrium (cor triatriatum sinistrum) or right atrium (cor triatriatum dextrum) is divided into two parts by a fold of tissue, a membrane, or a fibromuscular band. As far as division of the morphologically left atrium (cor triatriatum) is a recognized clinical and surgical entity. Division of the right atrium (prominence of the eustachian and thebesian valves) is recognized pathologically, but is rare. A partition division the right atrium was attached to the orifice of the inferior caval vei. The dividing partition is placed between the systemic venous sinus and the distal part of the right atrium, made up of the vestibule and appendage. This report describes a case of a divided right atrium, associated with a large atrial septal defect and valvular pulmonary stenosis.
More Related Videos
Related Concept Videos
Imaging Studies for Cardiovascular System II:Types of Echocardiography
Types of Echocardiography
Transthoracic Echocardiography (TTE)
TTE is the most common type of echocardiogram which involves placing a transducer on the patient's chest, emitting sound waves to create heart images. TTE is invaluable for evaluating the heart's size, structure, and motion, making it particularly useful for diagnosing...
Rheumatic Heart Disease II: Clinical Manifestations and Diagnostic Studies
Chambers of the Heart
Deoxygenated blood from the body is received in the right...
Mitral Stenosis II: Clinical features and Diagnostic Tests
Aortic Regurgitation II: Clinical Features and Diagnostic Tests
Cardiac Catheterization II: Right Heart Catheterization

