Charitos Efstratios I, Nienaber Christoph A, Sievers Hans-Hinrich
Cardiac and Thoracic Vascular Surgery Clinic, University Clinic of Schleswig-Holstein, Campus Luebeck, Ratzeburger Allee 160, 23538 Luebeck, Germany.
Interact Cardiovasc Thorac Surg. 2010 Sep;11(3):351-3. doi: 10.1510/icvts.2010.240705. Epub 2010 Jun 15.
A 48-year-old patient with Marfan syndrome presented with an ascending aortic and arch periprosthesis hematoma (14.0 x 9.0 cm) and a descending aortic aneurysm (8.7 x 9.1 cm) developed over the last 2.5 years, after several operations on the ascending aorta and arch as well as stent-graft placement in the descending aorta. After a diagnostic odyssey, the small true aortic lumen was identified as the source for the ascending aortic periprosthesis hematoma and descending aortic aneurysm expansion. The present case report underlines several important issues in the combined surgical and interventional management of patients requiring multiple and complex procedures on the thoracic aorta.
一名48岁的马凡综合征患者,在升主动脉和主动脉弓多次手术后以及降主动脉置入支架移植物后,在过去2.5年中出现了升主动脉和主动脉弓人工血管周围血肿(14.0×9.0 cm)以及降主动脉瘤(8.7×9.1 cm)。经过一番诊断探索,发现小的真性主动脉腔是升主动脉人工血管周围血肿和降主动脉瘤扩张的根源。本病例报告强调了在对需要对胸主动脉进行多次复杂手术的患者进行联合手术和介入治疗时的几个重要问题。