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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

Part of: Cardiac Morphology

Published online by Cambridge University Press:  06 January 2022

Otohime Mori Open the ORCID record for Otohime Mori [Opens in a new window] ,
Keiichi Fujiwara  and
Hisanori Sakazaki
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: [email protected]
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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.

Keywords

PHACE syndromecoarctation of the aortaaortic aneurysmductus arteriosus
Type
Brief Report
Information
Cardiology in the Young , Volume 32 , Issue 8 , August 2022 , pp. 1360 - 1362
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Copyright
© The Author(s), 2022. Published by Cambridge University Press

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References

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