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A rare combination of post-ductal coarctation of the aorta and adjunct tortuous aneurysm: a neonate with Posterior fossa anomalies, Haemangiomas of the head and neck, Arterial, Cardiovascular, and Eye anomalies and ventral developmental defect syndrome

Published online by Cambridge University Press:  06 January 2022

Otohime Mori*
Affiliation:
Department of Cardiovascular Surgery, Hyogo Prefectural Amagasaki General Medical Center, Hyogo, Japan
Keiichi Fujiwara
Affiliation:
Department of Cardiovascular Surgery, Hyogo Prefectural Amagasaki General Medical Center, Hyogo, Japan
Hisanori Sakazaki
Affiliation:
Department of Pediatric cardiology, Hyogo Prefectural Amagasaki General Medical Center, Hyogo, Japan
*
Author for correspondence: Otohime Mori, MD, Department of Cardiovascular Surgery, Hyogo Prefectural Amagasaki General Medical Center, 2-17-77, Higashi-Naniwa, Amagasaki, Hyogo, 660-8550, Japan. Tel: +81 6 6480 7000; Fax: +81 6 6480 7001. E-mail: ottotto_k@yahoo.co.jp

Abstract

A 4-day-old girl with Posterior fossa anomalies, Haemangiomas of the head and neck, Arterial, Cardiovascular, and Eye anomalies and ventral developmental defect syndrome comprising a facial haemangioma, aortic coarctation at the aortic arch, torturous aortic aneurysm distal to coarctation, and ductus arteriosus originating proximal to the coarctation is presented. The aortic arch was successfully reconstructed without cardiopulmonary bypass, and she is currently doing well after 4 years and 8 months.

Type
Brief Report
Copyright
© The Author(s), 2022. Published by Cambridge University Press

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References

Frieden, IJ, Reese, V, syndrome, Cohen DPHACE. The association of posterior fossa brain malformations, hemangiomas, arterial anomalies, coarctation of the aorta and cardiac defects, and eye abnormalities. Arch Dermatol 1996; 132: 307311.CrossRefGoogle ScholarPubMed
Metry, D, Heyer, G, Hess, C, et al. Consensus statement on diagnostic criteria for PHACE syndrome. Pediatrics 2009; 124: 14471456.CrossRefGoogle ScholarPubMed
Bayer, ML, Frommelt, PC, Blei, F, et al. Congenital cardiac, aortic arch, and vascular bed anomalies in PHACE syndrome (from the international PHACE syndrome registry). Am J Cardiol 2013; 112: 19481952.CrossRefGoogle Scholar
Caragher, SP, Scott, JP, Siegel, DH, et al. Aortic arch repair in children with PHACE syndrome. J Thorac Cardiovasc Surg 2016; 152: 709717.CrossRefGoogle ScholarPubMed
Sharma, B, Reddy, AK, Ganigara, M, et al. Aortic arch tortuosity with PHACE syndrome-a rare case scenario. Images Paediatr Cardio 2016; 18: 14.Google ScholarPubMed
Mery, CM. Aortic arch anomalies in PHACE syndrome: an individualized approach to an unusual problem. J Thorac Cardiovasc Surg 2016; 152: 718719.CrossRefGoogle Scholar
Al-Khaldi, A, Alhabshan, F, Tamimi, O, et al. Repair of aortic arch atresia with diffuse hypoplasia of the descending thoracic aorta. Eur J Cardiothorac Surg 2008; 33: 751753.CrossRefGoogle ScholarPubMed

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A rare combination of post-ductal coarctation of the aorta and adjunct tortuous aneurysm: a neonate with Posterior fossa anomalies, Haemangiomas of the head and neck, Arterial, Cardiovascular, and Eye anomalies and ventral developmental defect syndrome
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A rare combination of post-ductal coarctation of the aorta and adjunct tortuous aneurysm: a neonate with Posterior fossa anomalies, Haemangiomas of the head and neck, Arterial, Cardiovascular, and Eye anomalies and ventral developmental defect syndrome
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A rare combination of post-ductal coarctation of the aorta and adjunct tortuous aneurysm: a neonate with Posterior fossa anomalies, Haemangiomas of the head and neck, Arterial, Cardiovascular, and Eye anomalies and ventral developmental defect syndrome
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