Sugawara Y, Shimakura T, Kihara S, Tanaka S, Saitoh N, Imamaki M
Fukuyama Cardiovascular Hospital, Hiroshima, Japan.
Jpn J Thorac Cardiovasc Surg. 1998 Oct;46(10):1041-6. doi: 10.1007/BF03217871.
A 44-year-old male with Marfan's syndrome had undergone an initial operation for DeBakey type I acute aortic dissection with annulo-aortic ectasia. He had undergone replacement of the ascending aorta and aortic valve with a composite graft and reconstruction of the coronary artery by the Cabrol procedure. At 5 years after the initial surgery he experienced chest pain and was subsequently examined. Computed tomography revealed a pseudoaneurysm in the ascending aorta and the residual aortic dissection. The maximum diameter of the pseudoaneurysm was 85 mm and the maximum diameter of the aortic arch was 55 mm. The aortic arch was associated with an aberrant right subclavian artery. Angiography revealed that the pseudoaneurysm was caused by leakage at the coronary ostium-graft anastomoses. We repaired the anastomoses and performed total aortic arch replacement with reconstruction of four arch branches. The postoperative course was uneventful without any complications. We report this case because there have been few reports regarding arch replacement in cases with an aberrant right subclavian artery.
一名44岁患有马凡综合征的男性因I型DeBakey急性主动脉夹层合并主动脉瓣环扩张接受了初次手术。他接受了升主动脉和主动脉瓣的复合人工血管置换,并通过Cabrol手术重建了冠状动脉。初次手术后5年,他出现胸痛,随后接受检查。计算机断层扫描显示升主动脉有假性动脉瘤及残留主动脉夹层。假性动脉瘤最大直径为85mm,主动脉弓最大直径为55mm。主动脉弓合并右锁骨下动脉异常。血管造影显示假性动脉瘤是由冠状动脉开口-人工血管吻合口漏血引起的。我们修复了吻合口,并进行了全主动脉弓置换及四个弓分支的重建。术后过程顺利,无任何并发症。我们报告此病例是因为关于右锁骨下动脉异常病例的主动脉弓置换报道较少。