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家族性主动脉夹层：罕见家族聚集病例报告。

Familial aortic dissection: a report of rare family cluster.

作者信息

Toyama M, Amano A, Kameda T

机构信息

Department of Cardiovascular Surgery, Kameda General Hospital, Chiba, Japan.

出版信息

Br Heart J. 1989 Feb;61(2):204-7. doi: 10.1136/hrt.61.2.204.

DOI:10.1136/hrt.61.2.204
PMID:2923761
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1216642/
Abstract

Acute aortic dissection occurred in three of four siblings without Marfan syndrome. All of them were successfully treated by operation and remain well 6-42 months after operation. Their mother died suddenly in another hospital of acute aortic dissection. All her siblings were dead and cardiovascular disease was suspected in all of them.

摘要

4名无马方综合征的兄弟姐妹中有3人发生急性主动脉夹层。他们均成功接受了手术治疗，术后6至42个月情况良好。他们的母亲在另一家医院因急性主动脉夹层突然去世。她所有的兄弟姐妹均已去世，且均怀疑患有心血管疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ce1/1216642/ee59afde8d0e/brheartj00062-0074-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ce1/1216642/c716a5ee430f/brheartj00062-0072-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ce1/1216642/4a9cccc6cbaf/brheartj00062-0073-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ce1/1216642/f72084925331/brheartj00062-0073-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ce1/1216642/21371e781612/brheartj00062-0073-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ce1/1216642/ee59afde8d0e/brheartj00062-0074-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ce1/1216642/c716a5ee430f/brheartj00062-0072-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ce1/1216642/4a9cccc6cbaf/brheartj00062-0073-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ce1/1216642/f72084925331/brheartj00062-0073-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ce1/1216642/21371e781612/brheartj00062-0073-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ce1/1216642/ee59afde8d0e/brheartj00062-0074-a.jpg

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引用本文的文献

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A Gly1127Ser mutation in an EGF-like domain of the fibrillin-1 gene is a risk factor for ascending aortic aneurysm and dissection.原纤维蛋白-1基因的表皮生长因子样结构域中的Gly1127Ser突变是升主动脉瘤和主动脉夹层的一个危险因素。
Am J Hum Genet. 1995 Jun;56(6):1287-96.

本文引用的文献

1
Dissecting aneurysm o the aorta in mother and child.母婴主动脉夹层动脉瘤
Br Heart J. 1951 Jul;13(3):364-8. doi: 10.1136/hrt.13.3.364.
2
Dissecting aortic aneurysm in Marfan's syndrome.马方综合征中的主动脉夹层动脉瘤
Lancet. 1954 Oct 16;267(6842):791-2. doi: 10.1016/s0140-6736(54)92505-2.
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Dissecting aneurysm of the aorta; review of 29 cases.主动脉夹层动脉瘤；29例病例回顾
Glasgow Med J. 1952 Aug;33(8):320-30.
4
Multiple aortic aneurysms (thoracic and abdominal) in twins with Marfan's syndrome: fatal rupture during pregnancy.
J Thorac Cardiovasc Surg. 1967 Feb;53(2):223-30.
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Familial dissecting aneurysm complicating Marfan's syndrome.家族性夹层动脉瘤并发马方综合征。
Am Heart J. 1969 Oct;78(4):577-8. doi: 10.1016/0002-8703(69)90497-9.
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Dissecting aneurysm complicating Marfan's syndrome (arachnodactyly) in a mother and son.
Am Heart J. 1969 Mar;77(3):301-6. doi: 10.1016/0002-8703(69)90185-9.
7
Familial dissecting aortic aneurysm. A report of three cases within two generations.家族性主动脉夹层动脉瘤。两代内三例报告。
Br Heart J. 1967 Nov;29(6):852-8. doi: 10.1136/hrt.29.6.852.
8
Aortic dissection in more than one family member.不止一名家庭成员患有主动脉夹层。
Am J Cardiol. 1985 Jan 1;55(1):236-8. doi: 10.1016/0002-9149(85)90342-x.
9
Familial aortic dissection with iris anomalies--a new connective tissue disease syndrome?伴有虹膜异常的家族性主动脉夹层——一种新的结缔组织病综合征？
Birth Defects Orig Artic Ser. 1976;12(5):229-34.