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Computed tomography features of cor triatriatum: an institutional review
Archita Goel1, Sanjaya Viswamitra1, Bhavana Nagabhushana Reddy1
1Department of Radiology, Sri Sathya Sai Institute of Higher Medical Sciences, Bengaluru, India.
Insights
Cor Triatriatum is a rare congenital heart anomaly. Cardiac CT effectively identifies Cor Triatriatum Sinister and Dexter, aiding in diagnosis and management of associated cardiac conditions.
Area of Science:
- Cardiology
- Medical Imaging
- Congenital Heart Disease
Background:
- Cor Triatriatum is a rare congenital cardiac anomaly involving atrial septation.
- Preoperative diagnosis is crucial for effective patient management.
- This condition can manifest in the left (Cor Triatriatum Sinister - CTS) or right atrium (Cor Triatriatum Dexter - CTD).
Purpose of the Study:
- To review imaging findings of Cor Triatriatum.
- To classify the subtypes of Cor Triatriatum.
- To identify associated congenital cardiac anomalies influencing patient management.
Main Methods:
- Retrospective review of 10 Cor Triatriatum patients from EHR database.
- Cardiac CT imaging analysis for congenital heart disease.
- Analysis of medical records and imaging findings.
Main Results:
- Nine patients (90%) had CTS, one (10%) had CTD.
- CTS Type II and III were observed, with varying membrane orifice sizes.
- Pulmonary vein dilation and common associated anomalies like ASD and VSD were noted.
Conclusions:
- Cardiac CT provides excellent pre-operative evaluation for Cor Triatriatum.
- CT is effective for diagnosing, classifying, and identifying associated anomalies and complications.
Objectives:
Cor Triatriatum is a rare anomaly that can either involves the left atrium (Cor Triatriatum Sinister-CTS) or the right atrium (Cor Triatriatum Dexter- CTD). Preoperative identification of this anomaly is important in determining patient treatment course. The objective of this paper is to understand imaging findings, classification and to familiarise the reader with other associated congenital cardiac anomalies that influence patient management.
Methods:
From the hospital electronic health records (EHR) database, we identified 10 patients of Cor Triatriatum out of 974 patients who underwent cardiac CT between 15 July 2014 and 20 March 2020 for congenital heart disease. Medical records and imaging findings were reviewed retrospectively.
Results:
Out of 10 patients, nine patients had CTS (90%) and only one patient had CTD (10%). Five out of nine patients (55.5%) had CTS type II and four (44.4%) had CTS type III. The mean of the membrane orifices in CTS type III was 18.5 mm and was 5.78 mm in CTS type II. Pulmonary veins were dilated in all patients of CTS type II (62.5%), two patient of CTS type III (25%) and in only patient with CTD (12.5%). Ostium secundum atrial septal defect was the most common (66%) associated cardiac anomaly, followed by ventricular septal defect (44%).
Conclusions:
CT allows excellent pre-operative evaluation of Cor Triatriatum and associated cardiac anomalies.
Advances In Knowledge:
CT is excellent in making a diagnosis and classifying Cor Triatriatum and for identification of cardiac anomalies and complications associated with it.
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