Sbizzera Marc, Pozzi Matteo, Cosset Benoit, Koffel Catherine, Obadia Jean François, Robin Jacques
1 Department of Cardiac Surgery, 2 Department of Anesthesia and ICU "Louis Pradel" Cardiologic Hospital, "Claude Bernard" University, Lyon, France.
J Thorac Dis. 2016 Mar;8(3):E232-4. doi: 10.21037/jtd.2016.02.28.
Laubry-Pezzi syndrome is a rare congenital heart disease (CHD) combining a ventricular septal defect (VSD) and an aortic regurgitation (AR) due to a prolapse of the right coronary or, less frequently, non-coronary cusp. In the literature there are very few reports of long-term complications after surgical correction of this syndrome. We present the late occurrence of an aortic root pseudoaneurysm and a residual VSD in a patient with Laubry-Pezzi syndrome operated during childhood.
劳布里-佩齐综合征是一种罕见的先天性心脏病（CHD），合并室间隔缺损（VSD）和由于右冠状动脉瓣脱垂导致的主动脉瓣反流（AR），较少见的情况是无冠状动脉瓣脱垂。文献中关于该综合征手术矫正后长期并发症的报道非常少。我们报告了一名儿童期接受手术的劳布里-佩齐综合征患者晚期出现主动脉根部假性动脉瘤和残余室间隔缺损的情况。
