Suppr超能文献

家族性先天性二叶式主动脉瓣:继发性钙化性主动脉瓣狭窄和主动脉瘤。

Familial congenital bicuspid aortic valve: secondary calcific aortic stenosis and aortic aneurysm.

作者信息

Gale A N, McKusick V A, Hutchins G M, Gott V L

出版信息

Chest. 1977 Nov;72(5):668-70. doi: 10.1378/chest.72.5.668.

Abstract

A patient with an aneurysm of the ascending aorta and calcific stenosis of a congenital bicuspid aortic valve, whose brother also had a stenotic congenital bicuspid aortic valve, is described. Predominant aortic stenosis at cardiac catheterization and the presence of an aneurysm distal to and not including the aortic valvular ring made the initial diagnosis of Marfan's syndrome unlikely. Cystic medial necrosis present in the aneurysmal wall probably arose as a consequence of poststenotic dilation. Adequate noninvasive evaluation of the ascending aorta requires echocardiographic studies, as well as a chest x-ray film.

摘要

本文描述了一名患有升主动脉瘤和先天性二叶式主动脉瓣钙化狭窄的患者,其兄弟也患有狭窄性先天性二叶式主动脉瓣。心导管检查显示主要为主动脉瓣狭窄,且动脉瘤位于主动脉瓣环远端且不包括该瓣环,这使得马方综合征的初步诊断不太可能。动脉瘤壁中存在的囊性中层坏死可能是狭窄后扩张的结果。对升主动脉进行充分的非侵入性评估需要超声心动图检查以及胸部X光片。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验