Koushima R, Kikuchi Y, Sakurada T, Kusajima K
Department of Cardiovascular Surgery, National Obihiro Hospital, Hokkaido, Japan.
Jpn J Thorac Cardiovasc Surg. 1998 Nov;46(11):1190-3. doi: 10.1007/BF03217900.
We report a rare case of Stanford type A acute aortic dissection associated with a distal aortic arch atherosclerotic aneurysm. A 71-year-old female was referred to us with the diagnosis of thrombosed Stanford type A acute aortic dissection, however on the next day transesophageal echocardiography revealed the false lumen has been recanalized. In the operation, there was a distal aortic arch atherosclerotic aneurysm which was unidentified at the preoperation. It is very rare that the dissection originated from atherosclerotic aneurysm and proceeded to proximal and distal portion of the aorta.
我们报告了一例罕见的与远端主动脉弓动脉粥样硬化性动脉瘤相关的斯坦福A型急性主动脉夹层病例。一名71岁女性因诊断为血栓形成的斯坦福A型急性主动脉夹层被转诊至我院,然而第二天经食管超声心动图显示假腔已再通。手术中发现有一个术前未被识别的远端主动脉弓动脉粥样硬化性动脉瘤。夹层起源于动脉粥样硬化性动脉瘤并累及主动脉近端和远端的情况非常罕见。