Cuttone Fabio, Hadeed Khaled, Lacour-Gayet François, Lucron Hugues, Hascoet Sebastien, Acar Philippe, Leobon Bertrand, Van Praagh Richard
Department of Cardiac Surgery, University Hospital (CHU), Toulouse, France.
Department of Pediatric Cardiology, University Hospital (CHU), Toulouse, France.
Interact Cardiovasc Thorac Surg. 2017 May 1;24(5):772-777. doi: 10.1093/icvts/ivx006.
Leftward displacement of the septum primum is usually described as associated with hypoplastic left heart syndrome or visceral heterotaxy. This rare malformation results in partially or totally anomalous pulmonary venous drainage with a normal connection of the pulmonary veins to the left atrium, depending on the degree of septal shift. We report the 3D echocardiographic and anatomic findings as well as the surgical repair in a series of isolated severe leftward displacement of the septum primum, responsible for totally anomalous pulmonary venous drainage.
Three patients presenting with situs solitus and extreme leftward displacement of the septum primum were included. All of the pulmonary veins drained anomalously into the anatomical right atrium, and the distance between the mitral valve and the abnormal septum primum was greatly reduced, compromising the size of the left atrial chamber, but with normal left ventricle diameters. Preoperative 3D echocardiographic findings are reported. We achieved a biventricular surgical repair in all cases. The atrial septation was accomplished using an autologous pericardial patch after removing the abnormal septal membrane.
The postoperative course was free from any cardiovascular complications. Echocardiographic scans showed a harmonious reconstruction without pulmonary venous obstructions or stenosis.
This article reports the severe leftward displacement of the septum primum presented as an isolated cardiac malformation; 3D transthoracic echocardiography allowed an accurate diagnosis of this malformation and helped in choosing the best surgical strategy.
原发隔向左移位通常被描述为与左心发育不全综合征或内脏异位有关。这种罕见的畸形会导致部分或完全性肺静脉异位引流,根据间隔移位的程度,肺静脉与左心房正常连接。我们报告了一系列孤立性严重原发隔向左移位导致完全性肺静脉异位引流的三维超声心动图和解剖学发现以及手术修复情况。
纳入3例心脏位置正常且原发隔极度向左移位的患者。所有肺静脉均异常引流至解剖学右心房,二尖瓣与异常原发隔之间的距离大幅缩短,影响左心房腔大小,但左心室直径正常。报告术前三维超声心动图检查结果。所有病例均实施双心室手术修复。在切除异常间隔膜后,使用自体心包补片完成房间隔造口术。
术后过程未出现任何心血管并发症。超声心动图扫描显示重建良好,无肺静脉梗阻或狭窄。
本文报告了以孤立性心脏畸形形式出现的严重原发隔向左移位;三维经胸超声心动图能够准确诊断这种畸形,并有助于选择最佳手术策略。