Austin Bethany A, Kwon Deborah H, Smedira Nicholas G, Thamilarasan Maran, Lever Harry M, Desai Milind Y
Department of Cardiovascular Medicine, Heart and Vascular Institute, Cleveland Clinic, Cleveland, OH 44195, USA.
J Am Soc Echocardiogr. 2009 Jan;22(1):105.e5-6. doi: 10.1016/j.echo.2008.10.022.
We report the case of a symptomatic 18-year-old patient, gene-positive for hypertrophic cardiomyopathy (HCM), who presented with symptomatic dynamic left ventricular outflow tract (LVOT) obstruction caused by an abnormally thickened papillary muscle in the absence of septal hypertrophy. This was confirmed using multimodality imaging, including echocardiography and magnetic resonance imaging. He successfully underwent surgery for papillary muscle realignment without septal myectomy.
我们报告了一例18岁有症状的肥厚型心肌病(HCM)基因阳性患者,其在无室间隔肥厚的情况下,因乳头肌异常增厚导致有症状的动态左心室流出道(LVOT)梗阻。这通过包括超声心动图和磁共振成像在内的多模态成像得以证实。他成功接受了乳头肌复位手术,未进行室间隔心肌切除术。