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在先天性双叶主动脉瓣合并右冠状动脉异常的情况下实施Ross手术。

The Ross procedure performed in the setting of congenitally bifoliate aortic valve with anomalous right coronary artery.

作者信息

Morikawa Masayuki, Bando Ko, Sato Shinji

机构信息

Department of Thoracic and Cardiovascular Surgery, Sapporo Medical University School of Medicine, Sapporo, Hokkaido 060-8543, Japan.

出版信息

Cardiol Young. 2005 Apr;15(2):213-5. doi: 10.1017/S1047951105000417.

Abstract

We treated successfully using the Ross procedure a 14-year old with a congenitally stenotic bifoliate aortic valve associated with anomalous origin of the right coronary artery. The anomalous artery arose from the same aortic sinus that gave rise to the main stem of the left coronary artery, and reached the right atrioventricular groove by traversing the tissue plane between the aortic root and the subpulmonary infundibulum. Both coronary arteries were reimplanted using a single arterial button.

摘要

我们成功地使用罗斯手术治疗了一名14岁的患者,该患者患有先天性狭窄的双叶主动脉瓣,并伴有右冠状动脉异常起源。异常动脉起源于发出左冠状动脉主干的同一主动脉窦,穿过主动脉根部与肺动脉下漏斗部之间的组织平面,到达右房室沟。两条冠状动脉均使用单个动脉纽扣进行了再植入。

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