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Updated: Feb 27, 2026

Echocardiographic Evaluation of Atrial Communications before Transcatheter Closure
Published on: February 8, 2022
Obstructive neonatal atrial myxoma.
Federica Iezzi1, Andrea Quarti1, Alessandro Capestro1
1Department of Paediatric and Congenital Cardiac Surgery and Cardiology, Azienda Ospedaliero-Universitaria Ospedali Riuniti Ancona "Umberto I, G. M. Lancisi, G. Salesi" Ancona, Via Conca n. 71, 60128 Ancona, Italy.
Neonatal cardiac myxoma, a rare tumor, can obstruct blood flow. This case highlights successful surgical excision in a newborn, emphasizing the importance of recognizing rare pediatric cardiac tumors.
Area of Science:
- Pediatric Cardiology
- Cardiac Oncology
Background:
- Cardiac myxoma is the most common primary cardiac tumor in adults, but rare in neonates.
- Myxomas are endocardial masses, often attached to the interatrial septum, commonly in the left atrium.
- Understanding pediatric cardiac tumors is crucial as their types and epidemiology differ from adults.
Purpose of the Study:
- To report a rare case of neonatal cardiac myxoma.
- To highlight the successful surgical management of this rare condition.
Main Methods:
- Case report of a neonatal cardiac myxoma.
- Surgical excision of the tumor.
Main Results:
- A rare neonatal cardiac myxoma arising from the interatrial septum was identified.
- The myxoma caused significant mechanical obstruction of blood flow through the tricuspid valve.
- Successful surgical excision resulted in an uneventful recovery.
Conclusions:
- Large neonatal myxoma is exceptionally rare.
- Surgical excision in the first day of life is infrequent.
- Early recognition and management of pediatric cardiac tumors are vital.
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