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[发育不全的尖瓣导致左冠状动脉口狭窄]

[Stenosis of left coronary artery ostium by a hypoplastic cusp].

作者信息

Yashima Masafumi, Takeuchi T, Watanabe N, Kuwahara T, Kuwabara N, Goto H, Sakaguchi H

机构信息

Department of Pediatric Cardiac Surgery, Gifu Prefectural General Medical Center, Gifu, Japan.

出版信息

Kyobu Geka. 2009 May;62(5):354-7.

Abstract

Occlusion of a coronary ostium due to fusion of the aortic cusp to the aortic wall is a rare but noteworthy anomaly, because it may cause a sudden death. We report a 9-year-old girl with severe stenosis of the left coronary ostium by the aortic cusp that fused to the aortic wall. The left coronary flow was restored by excision of the adherent left aortic cusp, and aortic valve replacement was performed with the technique of bilateral enlargement of the aortic valve ring (Yamaguchi's method) to prevent prosthesis-patient mismatch in the future. The patient had an uneventful recovery and was discharged 14th postoperative day (POD). Postoperative angiography showed no coronary ostial stenosis.

摘要

由于主动脉瓣叶与主动脉壁融合导致冠状动脉口闭塞是一种罕见但值得关注的异常情况,因为它可能导致猝死。我们报告一名9岁女孩,其左冠状动脉口因主动脉瓣叶与主动脉壁融合而严重狭窄。通过切除粘连的左主动脉瓣叶恢复了左冠状动脉血流,并采用主动脉瓣环双侧扩大技术(山口法)进行主动脉瓣置换,以防止未来人工瓣膜与患者不匹配。患者恢复顺利,术后第14天出院。术后血管造影显示冠状动脉口无狭窄。

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