Leaking thoraco-abdominal aortic aneurysm in Marfan syndrome

Wong Cc, Ting Albert Cw, Chen Wk
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Abstract

Marfan syndrome is a congenital disorder of the connective tissue involving the ocular, skeletal and cardiovascular systems. Cardiovascular complications account mainly for the reduced life expectancy of patients with Marfan syndrome. Thoracic aortic aneurysms usually occur as a result of proximal aortic dissection but aneurysms of the descending aorta are infrequent. We report on a patient with rupture of an extensive thoraco-abdominal aortic aneurysm (Crawford type III) with a concomitant chronic thoracic aortic dissection (Stanford type A), treated successfully with aneurysmectomy and visceral artery reconstruction. Subsequent surgical intervention for the concomitant chronic thoracic aortic dissection was also performed. The importance of life-long surveillance of the cardiovascular system is highlighted.
马凡氏综合征的胸腹主动脉瘤漏出
马凡氏综合征是一种先天性结缔组织疾病,累及眼部、骨骼和心血管系统。心血管并发症是马凡氏综合征患者预期寿命降低的主要原因。胸主动脉瘤通常发生于近端主动脉夹层,而降主动脉动脉瘤并不常见。我们报告了一例广泛胸腹主动脉瘤破裂(Crawford III型)并伴有慢性胸主动脉夹层(Stanford a型)的患者,通过动脉瘤切除术和内脏动脉重建成功治疗。随后的手术干预合并慢性胸主动脉夹层也进行了。强调了终身监测心血管系统的重要性。
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