Ho Chi-Lin, Liang Kae-Woei, Fu Yun-Ching, Jan Sheng-Ling, Lin Ming-Chi, Chi Ching-Shiang, Hwang Betau
Section of Pediatric Cardiology, Department of Pediatrics, Taichung Veterans General Hospital, Taiwan, R.O.C.
J Chin Med Assoc. 2007 Jun;70(6):253-6. doi: 10.1016/S1726-4901(09)70369-7.
Lutembacher syndrome is a combination of congenital atrial septal defect (ASD) and acquired mitral stenosis (MS). The combination of these 2 diseases has hemodynamic influences on each other and the degree of MS may be underestimated. Traditionally, Lutembacher syndrome is corrected by surgical treatment. Nowadays, these 2 diseases are amenable to transcatheter treatment without the need for surgery. Here, we describe a 28-year-old female with Lutembacher syndrome who benefited from combined transcatheter therapy of balloon valvuloplasty for MS and device closure for ASD with an Amplatzer septal occluder.
鲁登巴赫综合征是先天性房间隔缺损（ASD）与后天性二尖瓣狭窄（MS）的组合。这两种疾病的组合对彼此有血流动力学影响，且二尖瓣狭窄的程度可能被低估。传统上，鲁登巴赫综合征通过手术治疗来矫正。如今，这两种疾病都可通过经导管治疗，无需进行手术。在此，我们描述一名患有鲁登巴赫综合征的28岁女性，她受益于二尖瓣狭窄球囊瓣膜成形术和使用Amplatzer房间隔封堵器封堵房间隔缺损的联合经导管治疗。
