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本文引用的文献

1
Endovascular treatment of ruptured axillary and large internal mammary artery aneurysms in a patient with Marfan syndrome.胸主动脉瘤患者合并马凡综合征，腋动脉和内乳动脉破裂的血管内治疗。
J Vasc Surg. 2011 Feb;53(2):478-82. doi: 10.1016/j.jvs.2010.08.076. Epub 2010 Nov 3.
2
The clinical spectrum of missense mutations of the first aspartic acid of cbEGF-like domains in fibrillin-1 including a recessive family.纤维连接素-1 中 cbEGF 样结构域第 1 个天冬氨酸错义突变的临床表型谱，包括一个常染色体隐性遗传家系。
Hum Mutat. 2010 Dec;31(12):E1915-27. doi: 10.1002/humu.21372.
3
The revised Ghent nosology for the Marfan syndrome.修订版马凡综合征根特分类法。
J Med Genet. 2010 Jul;47(7):476-85. doi: 10.1136/jmg.2009.072785.
4
Marfan's syndrome.马方综合征
Lancet. 2005 Dec 3;366(9501):1965-76. doi: 10.1016/S0140-6736(05)67789-6.
5
Endovascular treatment of a ruptured internal thoracic artery pseudoaneurysm presenting as a massive hemothorax in a patient with type I neurofibromatosis.对一名患有I型神经纤维瘤病、以大量血胸为表现的胸廓内动脉假性动脉瘤破裂进行血管内治疗。
Cardiovasc Intervent Radiol. 2005 Nov-Dec;28(6):818-21. doi: 10.1007/s00270-004-0067-8.
6
TGF beta signaling in health and disease.健康与疾病中的转化生长因子β信号传导
Nat Genet. 2004 Aug;36(8):790-2. doi: 10.1038/ng0804-790.
7
Heterozygous TGFBR2 mutations in Marfan syndrome.马凡综合征中的杂合型转化生长因子β受体2（TGFBR2）突变
Nat Genet. 2004 Aug;36(8):855-60. doi: 10.1038/ng1392. Epub 2004 Jul 4.
8
Phenotypic alteration of vascular smooth muscle cells precedes elastolysis in a mouse model of Marfan syndrome.在马凡综合征小鼠模型中，血管平滑肌细胞的表型改变先于弹性纤维溶解。
Circ Res. 2001 Jan 19;88(1):37-43. doi: 10.1161/01.res.88.1.37.
9
Internal mammary artery aneurysm in Marfan syndrome: case report.
Can Assoc Radiol J. 1999 Feb;50(1):47-50.
10
Aortic complications of Marfan's syndrome.马方综合征的主动脉并发症。
Lancet. 1998 Nov 28;352(9142):1722-3. doi: 10.1016/S0140-6736(05)79822-6.

马凡综合征患者双侧乳内动脉动脉瘤的血管内修复——病例报告

Endovascular Repair of Bilateral Internal Mammary Artery Aneurysms in a Patient with Marfan Syndrome-A Case Report.

作者信息

Alhawasli Hazem, Darki Amir, Lewis Bruce E

机构信息

Internal Medicine Department, Saint Joseph Hospital, Chicago, Illinois.

Division of Cardiology, Loyola University Medical Center, Chicago, Illinois.

出版信息

Int J Angiol. 2016 Dec;25(5):e39-e42. doi: 10.1055/s-0034-1378127. Epub 2014 Jun 24.

DOI:10.1055/s-0034-1378127
PMID:28031650
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5186218/
Abstract

Marfan syndrome (MFS) is an autosomal dominant condition that is caused by abnormal synthesis of connective tissue. The syndrome classically affects the ocular, musculoskeletal, and cardiovascular systems. The most common cardiovascular manifestations include mitral valve prolapse/regurgitation and aortic aneurysms at high risk of rupture and dissection. However, internal mammary artery (IMA) true aneurysms are rarely reported. In this case report, we describe a 43-year-old male patient with MFS and three previous thoracotomies referred for endovascular repair of bilateral IMA true aneurysms. To the best of our knowledge, there are no cases of endovascular treatment of bilateral IMA true aneurysms reported in the literature.

摘要

马凡综合征（MFS）是一种常染色体显性疾病，由结缔组织异常合成引起。该综合征典型地影响眼、肌肉骨骼和心血管系统。最常见的心血管表现包括二尖瓣脱垂/反流以及有破裂和夹层高风险的主动脉瘤。然而，胸廓内动脉（IMA）真性动脉瘤很少被报道。在本病例报告中，我们描述了一名43岁患有马凡综合征且曾接受过三次开胸手术的男性患者，因双侧IMA真性动脉瘤接受血管内修复治疗。据我们所知，文献中尚无双侧IMA真性动脉瘤血管内治疗的病例报道。