Suzuki Ryo, Mikamo Akihito, Kurazumi Hiroshi, Sato Masafumi, Ikeda Yoshitaka, Shirasawa Bungo, Hamano Kimikazu
Department of Cardiac Surgery, Yamaguchi University, Ube, Japan.
Kyobu Geka. 2011 Feb;64(2):99-104.
Marfan syndrome is an inherited connective tissue disorder with ocular, skeletal and cardiovascular systems and often causes acute aortic dissection. Interestingly, there have been several reports of familial thoracic aortic dissection in patients with autosomal dominant diseases without Marfan syndrome. Variation of the transforming growth factor-beta receptor (TGFBR) gene is reported to be one of the causes. We report a case of a familial aortic dissection not associated with Marfan syndrome, with mutation of TGFBR type 1. Hereditary aortic dissection of the non-Marfan syndrome that does not have clinical manifestations is not uncommon. Thus, the existence of familial aortic aneurysm should be in mind in diagnosis and treatment.
马凡综合征是一种遗传性结缔组织疾病,累及眼、骨骼和心血管系统,常导致急性主动脉夹层。有趣的是,有几篇报道称,患有非马凡综合征的常染色体显性疾病患者出现家族性胸主动脉夹层。据报道,转化生长因子-β受体(TGFBR)基因变异是病因之一。我们报告一例与马凡综合征无关的家族性主动脉夹层病例,该病例存在1型TGFBR突变。无临床表现的非马凡综合征遗传性主动脉夹层并不少见。因此,在诊断和治疗中应考虑家族性主动脉瘤的存在。