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马凡综合征患者主动脉修复术中并发严重不对称漏斗胸的处理

Management of severe asymmetric pectus excavatum complicating aortic repair in a patient with Marfan's syndrome.

作者信息

Yeung Jonathan C, Marcuzzi Danny, Peterson Mark D, Ko Michael A

机构信息

Division of Thoracic Surgery, St. Joseph's Health Centre, Toronto, ON, Canada.

Department of Radiology, St. Michael's Hospital, Toronto, ON, Canada.

出版信息

Interact Cardiovasc Thorac Surg. 2016 May;22(5):674-5. doi: 10.1093/icvts/ivv400. Epub 2016 Feb 13.

Abstract

We describe the case of a 28-year old man with Marfan's syndrome and severe pectus excavatum who required an aortic root replacement for an ascending aortic aneurysm. There was a near-vertical angulation of the sternum that presented challenges with opening and exposure of the heart during aortic surgery. Furthermore, removal of the sternal retractor after aortic repair resulted in sudden loss of cardiac output. A Ravitch procedure was then performed to successfully close the chest without further cardiovascular compromise. We propose that patients with a severe pectus excavatum and mediastinal displacement seen on preoperative CT scanning should be considered for simultaneous, elective repair.

摘要

我们描述了一名28岁患有马凡氏综合征和严重漏斗胸的男性病例,该患者因升主动脉瘤需要进行主动脉根部置换术。胸骨存在近乎垂直的成角,这给主动脉手术中心脏的打开和暴露带来了挑战。此外,主动脉修复后移除胸骨牵开器导致心输出量突然下降。随后进行了Ravitch手术,成功关闭胸腔,且未造成进一步的心血管损害。我们建议,对于术前CT扫描显示有严重漏斗胸和纵隔移位的患者,应考虑同时进行择期修复。

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