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一名患有主动脉弓中断的新生儿存在持续的第五主动脉弓:术中意外发现。

Persistent fifth aortic arch in a neonate with interrupted aortic arch: an unexpected intraoperative finding.

作者信息

Provost Bastien, Fournier Emmanuelle, Deng Mimi X, Belli Emre

机构信息

Department of Congenital Heart Diseases, Reference Center for Complex Congenital Cardiac Disease M3C, Marie Lannelongue Hospital, Plessis-Robinson, France.

Division of Cardiovascular Surgery, The Labatt Family Heart Center, The Hospital of Sick Children, Toronto, ON, Canada.

出版信息

Interdiscip Cardiovasc Thorac Surg. 2025 Jun 4;40(6). doi: 10.1093/icvts/ivaf145.

Abstract

Persistent fifth aortic arch (PFAA) is a rare variant of the aortic arch that may be associated with coarctation or interrupted aortic arch. We report the case of a neonate initially referred for coarctation repair. After a left thoracotomy was performed, a rare diagnosis of PFAA associated with interrupted aortic arch was made. Despite this unusual anatomy, the repair was successfully performed via a lateral approach. This unusual anatomy of the aortic arch deserves special consideration in case of association with coarctation. Indeed, repair from the side may not be possible due to the common origin of the neck-vessels, and resection should be extended as far as possible to eliminate remaining ductal tissue and prevent recoarctation.

摘要

持续性第五主动脉弓(PFAA)是一种罕见的主动脉弓变异,可能与主动脉缩窄或主动脉弓中断有关。我们报告了一例最初因主动脉缩窄修复而转诊的新生儿病例。在进行左胸剖胸术后,诊断出罕见的与主动脉弓中断相关的PFAA。尽管存在这种不寻常的解剖结构,但通过外侧入路成功完成了修复。在与主动脉缩窄相关的情况下,这种不寻常的主动脉弓解剖结构值得特别关注。实际上,由于颈部血管的共同起源,从侧面进行修复可能不可行,并且切除应尽可能延伸以消除残留的导管组织并防止再狭窄。

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