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一名三岁患者中主动脉综合征的外科修复

Surgical repair of middle aortic syndrome in a three-year-old patient.

作者信息

Ayik Fatih, Engin Cagatay, Ertugay Serkan, Atay Yüksel

机构信息

Department of Cardiovascular Surgery, Ege University, Izmir, Turkey.

出版信息

J Card Surg. 2011 Nov;26(6):659-62. doi: 10.1111/j.1540-8191.2011.01322.x. Epub 2011 Oct 20.

Abstract

Middle aortic syndrome is a rare variation of aortic coarctation that is localized to the distal thoracic and abdominal aorta, and can involve the visceral and renal arteries. Irreversible organ damage and end-stage congestive heart failure may be the possible harmful complications of this disease in untreated patients. We report a three-year-old patient with diffuse thoracic and abdominal aorta hypoplasia treated with a thoracic to abdominal aortic bypass graft.

摘要

中段主动脉综合征是主动脉缩窄的一种罕见变异,局限于胸段远端和腹主动脉,可累及内脏动脉和肾动脉。未经治疗的患者可能出现不可逆的器官损害和终末期充血性心力衰竭等有害并发症。我们报告一例三岁弥漫性胸段和腹主动脉发育不全患者,接受了胸段至腹主动脉旁路移植术治疗。

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