Inno Goki, Takahashi Yosuke, Kato Yasuyuki, Sasaki Yasuyuki
Department of Cardiovascular Surgery, Osaka City General Hospital, 2-13-22 Miyakojimahondori, Miyakojima-ku, Osaka, 534-0021, Japan.
Gen Thorac Cardiovasc Surg. 2018 Nov;66(11):667-670. doi: 10.1007/s11748-018-0889-y. Epub 2018 Jan 25.
We report the successful surgical treatment of aortic regurgitation in a 27-year-old woman with Turner syndrome (TS) who was admitted with exacerbation of dyspnea on exertion. Echocardiography showed a bicuspid aortic valve with severe aortic regurgitation and computed tomography showed dilatation of the ascending aorta and aortic root. Due to the patient's low body surface area (due to TS), standard determination of aortic size was not possible; therefore, we used the reference curves of aortic diameters in children. Because of the possibility of fatal ascending aortic dissection and rupture, we performed concomitant aortic root remodeling and aortic valve repair.
我们报告了一名27岁患有特纳综合征(TS)的女性主动脉瓣关闭不全的成功手术治疗案例,该患者因劳力性呼吸困难加重入院。超声心动图显示二叶式主动脉瓣伴严重主动脉瓣关闭不全,计算机断层扫描显示升主动脉和主动脉根部扩张。由于患者体表面积较低(因TS所致),无法进行标准的主动脉大小测定;因此,我们使用了儿童主动脉直径的参考曲线。鉴于存在致命性升主动脉夹层和破裂的可能性,我们同时进行了主动脉根部重塑和主动脉瓣修复。