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一种罕见的主动脉导管后缩窄合并附属迂曲型动脉瘤：一种后颅窝畸形、头颈部血管瘤、动脉、心血管和眼部异常及腹侧发育缺陷综合征的新生儿。

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.

机构信息

Department of Cardiovascular Surgery, Hyogo Prefectural Amagasaki General Medical Center, Hyogo, Japan.

Department of Pediatric cardiology, Hyogo Prefectural Amagasaki General Medical Center, Hyogo, Japan.

出版信息

Cardiol Young. 2022 Aug;32(8):1360-1362. doi: 10.1017/S1047951121005102. Epub 2022 Jan 6.

DOI:10.1017/S1047951121005102
PMID:34986911
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.

摘要

一位 4 天大的女婴，患有后颅窝畸形、头颈部血管瘤、动脉、心血管和眼部异常以及腹侧发育缺陷综合征，包括面部血管瘤、主动脉弓缩窄、缩窄远端迂曲性主动脉瘤和起源于缩窄近端的动脉导管未闭。主动脉弓在无体外循环的情况下成功重建，目前在术后 4 年 8 个月后情况良好。

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