Cor Triatriatum Dexter: Embryology, Presentation and Management.

Pediatr CardiolJan 19, 2026 (epub)

Sarah Kerr, Amy Hong, Aarti Bhat

✦ AI-curated · Sources linked

Case in brief

A single-center series described four neonates with cor triatriatum dexter (CTD), a congenital anomaly caused by persistence of the right valve of the sinus venosus. Each presented with hypoxemia and failed critical congenital heart disease pulse oximetry screening. Echocardiography showed a redundant membrane in the right atrium, leading to the diagnosis. All underwent surgical repair at an average age of 21 days (range, 5–41 days) and weight of 4 kg (range, 3.4–4.5 kg). Mean postoperative stay was 6 days (range, 3–9 days). At follow-up, three patients had no cardiac symptoms and were taking no cardiac medications, up to 7 years after surgery.

What made this case unusual

In all four patients, neonatal hypoxemia and failed pulse oximetry screening led to echocardiographic recognition of CTD, which appeared as a redundant right atrial membrane.

Diagnostic / clinical pearl

In a neonate with hypoxemia and a failed critical congenital heart disease screen, echocardiography can identify CTD as a redundant membrane within the right atrium.

Why it matters

The authors favor individualized decisions between surgery and watchful waiting, while generally leaning toward early repair; their small series reported favorable postoperative courses and follow-up in the three patients available.

Source

Published in Pediatr Cardiol. This summary was written by xxcode from the publication's abstract and metadata. It is not peer reviewed and is not a substitute for the original article. For clinical decisions, review the original publication.

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AI-generated summaries may contain errors or omissions. Verify clinically important information with the original publication.

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