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An unusual cause of refractory persistent pulmonary hypertension of the newborn: anomalous origin of one pulmonary artery

Published online by Cambridge University Press:  18 July 2013

Nilufer Guzoglu*
Affiliation:
Division of Neonatology, Zekai Tahir Burak Maternity Teaching Hospital, Ankara, Turkey
Fatma Nur Sari
Affiliation:
Division of Neonatology, Zekai Tahir Burak Maternity Teaching Hospital, Ankara, Turkey
Nahide Altug
Affiliation:
Division of Neonatology, Zekai Tahir Burak Maternity Teaching Hospital, Ankara, Turkey
*
Correspondence to: N. Guzoglu, Talat Pasa Bulvari, Samanpazari, B1 Blok, Altındag/Ankara 06230, Turkey. Tel: 0090312 306 50 00; Fax: 0090312 312 49 31; E-mail: nguzoglu@gmail.com

Abstract

Persistent pulmonary hypertension of the newborn is a source of considerable mortality and morbidity. Anomalous origin of one pulmonary artery, an uncommon congenital cardiac malformation, is a rare cause of persistent pulmonary hypertension. Here, we report the case of a patient with an anomalous origin of one pulmonary artery from the innominate artery who presented with persistent pulmonary hypertension refractory to treatment.

Type
Brief Reports
Copyright
Copyright © Cambridge University Press 2013 

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