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Percutaneous treatment of a double-drainage scimitar-like syndrome

Published online by Cambridge University Press:  03 September 2021

Giovanni Meliota*
Affiliation:
Pediatric Cardiology, Giovanni XXIII Pediatric Hospital, Bari, Italy
Pierluigi Zaza
Affiliation:
Pediatric Cardiology, Giovanni XXIII Pediatric Hospital, Bari, Italy
Ugo Vairo
Affiliation:
Pediatric Cardiology, Giovanni XXIII Pediatric Hospital, Bari, Italy
*
Author for correspondence: G. Meliota, MD, Pediatric Cardiology, Giovanni XXIII Pediatric Hospital, 207 Via Amendola, Bari70126, Italy. Tel: +39 080 5596698; Fax: +39 080 5596700. E-mail: giovanni.meliota@gmail.com

Abstract

Scimitar syndrome is a rare variant of anomalous right pulmonary vein connection to the inferior vena cava and it is associated with other cardiopulmonary anomalies. It generally requires surgery and sometimes it may go unrecognised into adulthood. We report a unique case of a scimitar syndrome variant in a young adult, who was successfully treated percutaneously, after the first misdiagnosis of arrhythmogenic ventricular cardiomyopathy. The cardiac magnetic resonance unveiled the uncommon anatomical pattern, avoiding surgical repair. Cross-sectional imaging is extremely useful in the diagnosis and treatment planning of CHD in adults.

Type
Brief Report
Copyright
© The Author(s), 2021. Published by Cambridge University Press

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References

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