class='kwd-title'>Keywords: Aortopathy, Aortic a'/> Profound Aortopathy: A Rare Case of Massive Ascending and Descending Aortic Aneurysms Type B Aortic Dissection and Severe Aortic Valve Regurgitation in an Adult Patient With Uncorrected Congenital Aortic Coarctation
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Profound Aortopathy: A Rare Case of Massive Ascending and Descending Aortic Aneurysms Type B Aortic Dissection and Severe Aortic Valve Regurgitation in an Adult Patient With Uncorrected Congenital Aortic Coarctation

机译:深刻的主动脉病变:未成年先天性主动脉缩窄的成年患者中发生大规模的升主动脉主动脉瘤和降主动脉瘤B型主动脉夹层和严重的主动脉瓣反流的病例

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摘要

class="kwd-title">Keywords: Aortopathy, Aortic aneurysm, Aortic coarctation, Aortic regurgitation, MRI class="head no_bottom_margin" id="sec1title">IntroductionAortic coarctation is one of the more common congenital cardiovascular abnormalities. However, uncorrected aortic coarctation is rarely encountered in adults. Furthermore, when present, aortic coarctation is most commonly associated with ascending aortic aneurysms. Here we present a case of a rare combination of massive ascending and descending thoracic aortic aneurysms (TAAs), type B aortic dissection, and severe aortic valve regurgitation further complicated by severe left ventricular (LV) systolic dysfunction in a patient with an uncorrected aortic coarctation. To our knowledge, this is the first known report with this combination and severity of aortopathy.
机译:<!-fig ft0-> <!-fig @ position =“ anchor” mode =文章f4-> <!-fig mode =“ anchred” f5-> <!-fig / graphic | fig / alternatives / graphic mode =“ anchored” m1-> class =“ kwd-title”>关键字:主动脉病变,主动脉瘤,主动脉缩窄,主动脉瓣关闭不全,MRI class =“ head no_bottom_margin” id =“ sec1title”>简介主动脉缩窄是较常见的先天性心血管异常之一。但是,成年人中很少见到未矫正的主动脉缩窄。此外,当存在时,主动脉缩窄最常与升主动脉瘤有关。在这里,我们介绍一例罕见的合并主动脉缩窄的患者,其合并了大面积的升主动脉和降主动脉瘤(TAA),B型主动脉夹层和严重的主动脉瓣关闭不全,并伴有严重的左心室(LV)收缩功能异常。 。就我们所知,这是主动脉病的这种结合和严重程度的第一个已知报告。

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