一种罕见的出生缺陷:二尖瓣干和卢索动脉

O. H. Marion, Akdi Khaoula, Boutakioute Badr, Ouali Idrissi Mariem, cherifidrissielganouni najat
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引用次数: 0

摘要

我们提出的情况下,一个50岁的妇女接受了CT扫描的胸部作为监测检查的一部分,在此期间,先天性异常的主动脉弓分支被发现。二颈动脉主干伴异常右锁骨下动脉,无其他异常血管排列。这种罕见的异常类型通常在儿童时期或症状出现时被发现。我们的病人不知道发生呼吸困难型呼吸障碍或吞咽困难型消化障碍。从来没有人向他报告过这种异常情况。教育临床医生关于这种异常是重要的心脏病学家和介入放射科医生鉴于越来越多的病例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Truncus Bicarotidus and Arteria Lusoria: A Rare Birth Defect
We present the case of a 50-year-old woman who underwent a CT scan of the chest as part of a surveillance examination during which a congenital anomaly of the branches of the aortic arch was discovered. It was a bicarotid trunk associated with an aberrant right subclavian artery, with no other abnormal vascular arrangement. This rare type of anomaly is usually discovered in childhood or when symptoms appear. Our patient had no knowledge of an episode of dyspnea-type respiratory disorder or dysphagia-type digestive disorder. This anomaly had never been reported to him. Educating clinicians about this anomaly is important for cardiologists and interventional radiologists given the growing number of cases.
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