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支架治疗“第五主动脉弓”缩窄:一种安全且有吸引力的手术替代疗法。

Stenting Coarctation of the "Fifth Aortic Arch": A Safe and Attractive Therapeutic Alternative to Surgery.

机构信息

Pediatric Cardiology and Pediatric Interventional Cardiology Department, Universitat Autònoma Barcelona, Hospital Vall d'Hebron, Barcelona, Spain.

Pediatric Cardiology Department, Universitat de Girona, Hospital Doctor Josep Trueta, Girona, Spain.

出版信息

World J Pediatr Congenit Heart Surg. 2020 Jul;11(4):NP140-NP143. doi: 10.1177/2150135117752895. Epub 2018 Apr 3.

Abstract

"Persistence of the fifth aortic arch" is a rare congenital cardiovascular anomaly that consists of an abnormal vessel arising from the distal ascending aorta connecting with the systemic or pulmonary circulation. We report a case of a type A interruption of the aortic arch and a coarctation of the fifth aortic arch, which connected the ascending with the descending aorta. No cardiac surgery was required because a covered stent was successfully implanted in the fifth aortic arch when the patient was 4 years old. A chromosome 9 q arm duplication of uncertain significance was also found, an anomaly never described before in this clinical context.

摘要

“第五主动脉弓永存”是一种罕见的先天性心血管畸形,由起源于升主动脉远端的异常血管引起,与体循环或肺循环相连。我们报告了一例主动脉弓中断伴第五主动脉弓缩窄的病例,该缩窄连接了升主动脉和降主动脉。由于患者 4 岁时成功植入了覆膜支架,因此无需心脏手术。还发现了一条意义未明的 9q 臂染色体重复,这在该临床情况下以前从未描述过。

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