Causes and histopathology of ascending aortic disease in children and young adults

被引:67
作者
Jain, Deepali [1 ]
Dietz, Harry C. [2 ,3 ,4 ,5 ,6 ]
Oswald, Gretchen L. [6 ]
Maleszewski, Joseph J. [7 ]
Halushka, Marc K. [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Pathol, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Dept Pediat, Baltimore, MD 21205 USA
[3] Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21205 USA
[4] Johns Hopkins Univ, Sch Med, Dept Mol Biol & Genet, Baltimore, MD 21205 USA
[5] Johns Hopkins Univ, Sch Med, Howard Hughes Med Inst, Baltimore, MD 21205 USA
[6] Johns Hopkins Univ, Sch Med, McKusick Nathans Inst Genet Med, Baltimore, MD 21205 USA
[7] Mayo Clin, Dept Lab Med & Pathol, Div Anat Pathol, Rochester, MN USA
关键词
Aortic aneurysm; Dissection; Genetic; SUDDEN-DEATH; CARDIOVASCULAR MANIFESTATIONS; CARDIAC MANIFESTATIONS; TAKAYASUS-ARTERITIS; SURGICAL PATHOLOGY; MISSENSE MUTATION; NATURAL-HISTORY; ROOT DILATATION; MARFAN-SYNDROME; TURNER-SYNDROME;
D O I
10.1016/j.carpath.2009.09.008
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Ascending aortic diseases (aneurysms, dissections, and stenosis) and associated aortic valve disease are rare but important causes of morbidity and mortality in children and young adults. Certain genetic causes, such as Marfan syndrome and congenital bicuspid aortic valve disease, are well known. However, other rarer genetic and nongenetic causes of aortic disease exist. Methods: We performed an extensive literature search to identify known causes of ascending aortic pathology in children and young adults. We catalogued both aortic pathologies and other defining systemic features of these diseases. Results: We describe 17 predominantly genetic entities that have been associated with thoracic aortic disease in this age group. Conclusions: While extensive literature on the common causes of ascending aortic disease exists, there is a need for better histologic documentation of aortic pathology in rarer diseases. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:15 / 25
页数:11
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