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马凡综合征合并主动脉瓣环扩张及急性A型主动脉夹层患者行保留主动脉瓣手术(David I型再植入术)进行主动脉根部重建。

Aortic root reconstruction by aortic valve-sparing operation (David type I reimplantation) in Marfan syndrome accompanied by annuloaortic ectasia and acute type-A aortic dissection.

作者信息

Inamura Shunichi, Furuya Hidekazu, Yagi Kentarou, Ikeya Eriko, Yamaguchi Masaomi, Fujimura Takabumi, Kanabuchi Kazuo

机构信息

Department of Cardiovascular Surgery, Tokai University School of Medicine, Tokai University Hospital, Isehara, Kanagawa, Japan.

出版信息

Tokai J Exp Clin Med. 2006 Sep 20;31(3):105-8.

Abstract

To reconstruct the aortic root for aneurysm of the ascending aorta accompanied by aortic regurgitation, annuloaortic ectasia (AAE) and acute type-A dissection with root destruction, the Bentall operation using a prosthetic valve still is the standard procedure today. Valve-sparing procedures have actively been used for aortic root lesions, and have also been attempted in aortic root reconstruction for Marfan syndrome which may have abnormalities in the valve leaflets. We conducted a valve-sparing procedure in a female patient with Marfan syndrome who had AAE accompanied by type-A acute aortic dissection. The patient was a 37-year-old woman complaining of severe pain from the chest to the back. The limbs were long, and funnel breast was observed. Diastolic murmurs were heard. On chest computed tomography, a dissection cavity was present from the ascending aorta to the left common iliac artery, and the root dilated to 55 mm. Grade II aortic regurgitation was observed on ultrasound cardiography. Regarding her family history, her father had died suddenly at 54 years of age. She was diagnosed with type-A acute dissection concurrent with Marfan syndrome and AAE. The structure of the aortic valve was normal, and root reconstruction by a valve-sparing operation and total replacement of the aortic arch was conducted. On postoperative ultrasound cardiography, the aortic regurgitation was within the allowable range, and the shortterm postoperative results were good.

摘要

对于升主动脉瘤合并主动脉瓣反流、瓣环主动脉扩张(AAE)以及根部破坏的急性A型主动脉夹层,使用人工瓣膜的Bentall手术至今仍是标准术式。保留瓣膜的手术已积极应用于主动脉根部病变,并且也已尝试用于可能存在瓣叶异常的马方综合征的主动脉根部重建。我们对一名患有AAE并伴有A型急性主动脉夹层的马方综合征女性患者实施了保留瓣膜手术。该患者为一名37岁女性,主诉胸部至背部剧痛。四肢修长,可见漏斗胸。可闻及舒张期杂音。胸部计算机断层扫描显示,从升主动脉至左髂总动脉存在一个夹层腔,根部直径扩张至55毫米。超声心动图显示为II级主动脉瓣反流。关于其家族史,她的父亲在54岁时突然去世。她被诊断为A型急性夹层并发马方综合征和AAE。主动脉瓣结构正常,通过保留瓣膜手术进行根部重建并对主动脉弓进行全置换。术后超声心动图显示,主动脉瓣反流在允许范围内,术后短期效果良好。

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