首页> 美国卫生研究院文献>The Journal of Tehran University Heart Center >Coarctation Stenting in a Rare Case with Congenitally Corrected Transposition of the Great Arteries and the Bicuspid Aortic Valve
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Coarctation Stenting in a Rare Case with Congenitally Corrected Transposition of the Great Arteries and the Bicuspid Aortic Valve

机译:在罕见的案例中缩短支撑并在伟大的动脉和双囊主动脉瓣膜中进行了先前校正的转子

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摘要

Congenitally corrected transposition of the great arteries (cc-TGA) is a rare congenital abnormality that occurs in 1 per 33000 live births. This abnormality comprises nearly 0.05% of all congenital heart defects, with at least 90% of cc-TGA patients having associated cardiac defects; some of these associated defects are, however, very rare. In this case report, we describe a 22-year-old man who referred to our hospital for the evaluation of hypertension and cardiac murmurs. Via echocardiography and catheterization, the patient was finally diagnosed with cc-TGA, bicuspid aortic valve, and coarctation of the aorta. He underwent successful percutaneous transarterial coarctoplasty without any complications at early and 6 months’ follow-up visits.
机译:最终校正的伟大动脉(CC-TGA)的转置是一种罕见的先天性异常,其出现在每33000个活产前的1个。这种异常包含近0.05%的全先天性心脏缺陷,具有至少90%的CC-TGA患者具有相关的心脏缺陷;然而,其中一些相关的缺陷是非常罕见的。在本案报告中,我们描述了一名22岁的男子,他们将医院提到评估高血压和心脏杂音。通过超声心动图和导管化,最终诊断患者用CC-TGA,双囊主动脉瓣和主动脉的缩窄。他在早期和6个月的后续访问时没有任何并发​​症的成功经皮横冲娱乐性成功。

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