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两名青少年息肉病综合征合并 SMAD4 基因突变患者的胸主动脉疾病。

Thoracic aortic disease in two patients with juvenile polyposis syndrome and SMAD4 mutations.

机构信息

MassGeneral Hospital for Children, Boston, MA, USA.

出版信息

Am J Med Genet A. 2013 Jan;161A(1):185-91. doi: 10.1002/ajmg.a.35659. Epub 2012 Dec 13.

Abstract

Dilation or aneurysm of the ascending aorta can progress to acute aortic dissection (Thoracic Aortic Aneurysms and Aortic Dissections, TAAD). Mutations in genes encoding TGF-β-related proteins (TGFBR1, TGFBR2, FBN1, and SMAD3) cause syndromic and inherited TAAD. SMAD4 mutations are associated with juvenile polyposis syndrome (JPS) and a combined JPS-hereditary hemorrhagic telangiectasia (HHT) known as JPS-HHT. A family with JPS-HHT was reported to have aortic root dilation and mitral valve abnormalities. We report on two patients with JPS-HHT with SMAD4 mutations associated with thoracic aortic disease. The first patient, an 11-year-old boy without Marfan syndrome features, had JPS and an apparently de novo SMAD4 mutation (c.1340_1367dup28). Echocardiography showed mild dilation of the aortic annulus and aortic root, and mild dilation of the sinotubular junction and ascending aorta. Computed tomography confirmed aortic dilation and showed small pulmonary arteriovenous malformations (PAVM). The second patient, a 34-year-old woman with colonic polyposis, HHT, and features of Marfan syndrome, had a SMAD4 mutation (c.1245_1248delCAGA). Echocardiography showed mild aortic root dilation. She also had PAVM and hepatic focal nodular hyperplasia. Her family history was significant for polyposis, HHT, thoracic aortic aneurysm, and dissection and skeletal features of Marfan syndrome in her father. These two cases confirm the association of thoracic aortic disease with JPS-HHT resulting from SMAD4 mutations. We propose that the thoracic aorta should be screened in patients with SMAD4 mutations to prevent untimely death from dissection. This report also confirms that SMAD4 mutations predispose to TAAD.

摘要

升主动脉扩张或动脉瘤可进展为急性主动脉夹层(胸主动脉瘤和主动脉夹层,TAAD)。编码 TGF-β相关蛋白(TGFBR1、TGFBR2、FBN1 和 SMAD3)的基因突变导致综合征性和遗传性 TAAD。SMAD4 突变与青少年息肉病综合征(JPS)和一种称为 JPS-HHT 的 JPS-遗传性出血性毛细血管扩张症(HHT)相关。据报道,一个 JPS-HHT 家族存在主动脉根部扩张和二尖瓣异常。我们报告了两例具有 SMAD4 突变的 JPS-HHT 患者,这些突变与胸主动脉疾病相关。第一例患者为 11 岁男孩,无马凡综合征特征,患有 JPS 和明显的新发 SMAD4 突变(c.1340_1367dup28)。超声心动图显示主动脉瓣环和主动脉根部轻度扩张,窦管交界处和升主动脉轻度扩张。计算机断层扫描证实了主动脉扩张,并显示小的肺动静脉畸形(PAVM)。第二例患者为 34 岁女性,患有结肠息肉、HHT 和马凡综合征特征,存在 SMAD4 突变(c.1245_1248delCAGA)。超声心动图显示主动脉根部轻度扩张。她还患有 PAVM 和肝局灶性结节性增生。她的家族史中有息肉病、HHT、胸主动脉瘤和夹层以及她父亲的马凡综合征骨骼特征的病史。这两例病例证实了 SMAD4 突变导致的 JPS-HHT 与胸主动脉疾病相关。我们建议对 SMAD4 突变患者进行胸主动脉筛查,以防止因夹层而意外死亡。本报告还证实 SMAD4 突变易导致 TAAD。

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