Behjatiardakani Mostafa, Rafiei Mansour, Nough Hossein, Rafiei Reza
Department of Pediatrics, Division of Pediatric Cardiology, Yazd University of Medical Science, Yazd, Iran.
Acta Med Iran. 2011;49(5):327-30.
Lutembacher syndrome refers to the rare combination of a congenital atrial septal defect and acquired mitral stenosis. Traditionally, Lutembacher syndrome has been corrected by surgical treatment. We describe two patients treated percutaneouly with a combined Inoue balloon valvuloplasty and septal defect closure using the Amplatzer septal occlusion device.
鲁腾巴赫综合征是指先天性房间隔缺损与后天性二尖瓣狭窄的罕见组合。传统上，鲁腾巴赫综合征通过手术治疗来矫正。我们描述了两名患者，他们接受了经皮治疗，采用了联合使用伊诺埃球囊瓣膜成形术和使用Amplatzer房间隔封堵装置关闭房间隔缺损的方法。
