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Abnormal drainage pathway of a supracardiac total anomalous pulmonary venous drainage in a neonate: a case report

Part of: Cardiac Morphology

Published online by Cambridge University Press:  04 May 2021

Johan A. Jamaluddin Open the ORCID record for Johan A. Jamaluddin [Opens in a new window]  and
Norliza Ali
Johan A. Jamaluddin*
Affiliation:
Department of Paediatrics, Faculty of Medicine & Health Sciences, Universiti Putra Malaysia, Serdang, Selangor, Malaysia
Norliza Ali
Affiliation:
Department of Paediatrics, Hospital Serdang, Serdang, Selangor, Malaysia
*
Author for correspondence: Dr Johan A. Jamaluddin, Department of Paediatrics, Faculty of Medicine & Health Sciences, Universiti Putra Malaysia, 43400 Serdang, Selangor, Malaysia. Tel: 60193875431; Fax: 89489369. E-mail: johanaref@yahoo.com.
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Abstract

Supracardiac total anomalous pulmonary venous drainage is commonly associated with a left-sided ascending vein draining into innominate vein. We present a case of a newborn with a right-sided ascending vein, draining into the right superior caval vein with stenosis at the SVC-ascending vein junction, posing a surgical dilemma in corrective surgery. Usage of three-dimensional computed tomographic scan was essential in delineating the anatomy and aiding surgery. The case demonstrates the rarity of this type of cardiac disease and the complications that develop.

Keywords

Supracardiac total anomalous pulmonary venous drainageascending veinright superior caval vein
Type
Original Article
Information
Cardiology in the Young , Volume 32 , Issue 1 , January 2022 , pp. 21 - 23
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Copyright
© The Author(s), 2021. Published by Cambridge University Press

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References

Seale, AN, Uemura, H, Webber, SA, et al British congenital cardiac association: total anomalous pulmonary venous connection: morphology and outcome from an international population-based study. Circulation 2010; 122: 2718–2726.CrossRefGoogle ScholarPubMed
Burroughs, JT, Edwards, JE. Total anomalous pulmonary venous connection. Am Heart J 1960; 59: 913–931.CrossRefGoogle ScholarPubMed
Karamlou, T, Gurofsky, R, Al Sukhni, E, et al Factors associated with mortality and reoperation in 377 children with total anomalous pulmonary venous connection. Circulation 2007; 115: 1591–1598.CrossRefGoogle ScholarPubMed
Hancock Friesen, CL, Zurakowski, D, Thiagarajan, RR, et al Total anomalous pulmonary venous connection: an analysis of current management strategies in a single institution. Ann Thorac Surg 2005; 79: 596–606.CrossRefGoogle ScholarPubMed
Casta, A, Wolf, WJ. Echo Doppler detection of external compression of the vertical vein causing obstruction in total anomalous pulmonary venous connection. Am Heart J 1988; 116: 1045–1047.CrossRefGoogle ScholarPubMed
DeLeon, SY, Freeman, JE, Ilbawi, MN, et al Surgical techniques in partial anomalous pulmonary veins to the superior vena cava. Ann Thorac Surg 1993; 55: 1222–1226.CrossRefGoogle Scholar
Sarıtaş, B, Bolat, B, Özkan, S, et al The effect of vertical vein and/or atrial septal defect which is left open in the correction of total anomalous pulmonary venous connection. Turk Gogus Kalp Dama 2008; 16: 6–10.Google Scholar