Suppr超能文献

先天性肺动脉瓣和漏斗部狭窄合并三尖瓣埃布斯坦畸形。病例报告。

Congenital pulmonary valvular and infundibular stenosis complicating Ebstein's anomaly of the tricuspid valve. A case report.

作者信息

Alipour M S, Shadkhoo G, Tarbiat C

出版信息

Jpn Heart J. 1980 Nov;21(6):883-90. doi: 10.1536/ihj.21.883.

Abstract

Clinical, hemodynamic, angiographic, and echocardiographic as well as operative findings of a 19 years old girl are presented who had the unique combination of severe pulmonary valvular and infundibular stenosis with Ebstein's anomaly of the tricuspid valve. Pulmonary stenosis was relieved by infundibular resection and valvotomy. The atrial septal defect was closed with plication of atrialized ventricle and insertion of a porcine tricuspid prosthesis. Recatheterization 2 months postoperatively revealed disappearance of characteristic angiographic findings and slight residual gradient.

摘要

本文报告了一名19岁女孩的临床、血流动力学、血管造影、超声心动图及手术所见,该患者患有严重的肺动脉瓣和漏斗部狭窄,并伴有三尖瓣埃布斯坦畸形这一独特组合。通过漏斗部切除术和瓣膜切开术缓解了肺动脉狭窄。采用心房化心室折叠术及植入猪三尖瓣假体闭合房间隔缺损。术后2个月复查心导管显示特征性血管造影表现消失,残余压差轻微。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验