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Published on: February 11, 2022
[Cor triatriatum--a case report]
Rafał Młynarski1, Eugeniusz Piłat, Anna Drzewiecka
1Klinika Elektrokardiologii, Slaska Akademia Medyczna, Katowice-Ochojec.
Insights
This case study details a 54-year-old female diagnosed with cor triatriatum. Echocardiography, both transthoracic and transesophageal, proved crucial in diagnosis.
Area of Science:
- Cardiology
- Medical Imaging
Background:
- Cor triatriatum is a rare congenital heart anomaly characterized by an accessory membrane dividing the left atrium.
- Early and accurate diagnosis is essential for appropriate management and to prevent complications.
Observation:
- A 54-year-old female presented with symptoms suggestive of cardiac pathology.
- Diagnostic workup included transthoracic echocardiography (TTE) and transesophageal echocardiography (TEE).
Findings:
- Echocardiography revealed the presence of cor triatriatum, accurately delineating the anomalous intra-atrial septum.
- Both TTE and TEE demonstrated their utility in visualizing the cardiac anatomy and identifying the specific malformation.
Implications:
- This case highlights the importance of echocardiography in diagnosing rare cardiac conditions like cor triatriatum.
- Effective utilization of echocardiographic modalities can lead to timely intervention and improved patient outcomes in complex congenital heart disease.
Abstract:
A case of a 54 year old female with cor tritriatum is described. Diagnostic role of transthoracic and transesophageal echocardiography is discussed.
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