Suppr超能文献

一名患有马凡综合征的青少年二尖瓣环大量钙化。病例报告。

Massive calcification of the mitral valve annulus in an adolescent with Marfan syndrome. A case report.

作者信息

Correia Joana, Rodrigues Dina, da Silva A Marinho, Sá e Melo Antonio, Providência Luîs A

机构信息

Unidade de Cardiologia Pediátrica do Serviço de Cardiologia, Hospital da Universidade de Coimbra, Coimbra, Portugal.

出版信息

Rev Port Cardiol. 2006 Oct;25(10):921-6.

Abstract

Marfan syndrome (MFS) is an inherited connective tissue disorder, transmitted as an autosomal dominant trait. Its phenotypic and clinical expression is variable and involves several body systems. The ocular, skeletal and cardiovascular systems are characteristically affected. Involvement of the cardiovascular system is the main cause of morbidity and mortality. The authors report the case of a thirteen-year-old girl, with MFS diagnosed at age five, referred to the pediatric cardiology department because of mitral regurgitation. In addition to severe mitral regurgitation due to prolapse of both mitral valve leaflets, diagnostic exams showed massive mitral annulus calcification and ostium secundum atrial septal defect (ASD). The patient underwent successful mitral valve repair and ASD closure surgery. In this report we highlight some features of MFS, stressing the cardiovascular aspects.

摘要

马凡综合征(MFS)是一种遗传性结缔组织疾病,以常染色体显性特征遗传。其表型和临床症状具有多样性,累及多个身体系统。眼部、骨骼和心血管系统通常会受到影响。心血管系统受累是发病和死亡的主要原因。作者报告了一例13岁女孩的病例,该女孩5岁时被诊断为马凡综合征,因二尖瓣反流转诊至儿科心脏病科。除了由于二尖瓣叶脱垂导致的严重二尖瓣反流外,诊断检查还显示有大量二尖瓣环钙化和继发孔房间隔缺损(ASD)。该患者成功接受了二尖瓣修复和房间隔缺损封堵手术。在本报告中,我们重点介绍马凡综合征的一些特征,着重强调心血管方面。

相似文献

引用本文的文献

1
Calcification of the heart: mechanisms and therapeutic avenues.
Expert Rev Cardiovasc Ther. 2018 Jul;16(7):527-536. doi: 10.1080/14779072.2018.1484282. Epub 2018 Jun 12.

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