Bogers A J, Rohmer J, Wolsky S A, Quaegebeur J M, Huysmans H A
Department of Thoracic Surgery, Thoraxcenter, University Hospital Dijkzigt, Rotterdam, The Netherlands.
Thorac Cardiovasc Surg. 1990 Feb;38(1):30-2. doi: 10.1055/s-2007-1013986.
Four patients are described with pulmonary atresia and ventricular septal defect, in whom the pulmonary circulation was dependent on a fistula from the left coronary artery to the pulmonary artery. The issue in this complex anomaly is complete preoperative diagnosis, including anatomic information on the coronary artery fistula and the pulmonary vasculature. This was achieved in the last 2 patients. In the last patient echocardiography turned out to be an important diagnostic tool in this rare anomaly and facilitated selective angiocardiography. All 4 patients were successfully operated by closing the fistula, closing other aortopulmonary connections and inserting a valved conduit between right ventricle and pulmonary artery. The ventricular septal defect was closed in 3 patients with a patch. In the setting of an already existing pulmonary hypertension and a possibly inadequate pulmonary arterial system at surgery, a perforated patch was inserted in the ventricular septal defect of the remaining patient.
本文描述了4例患有肺动脉闭锁和室间隔缺损的患者,其肺循环依赖于左冠状动脉至肺动脉的瘘管。这种复杂畸形的关键问题是术前的完整诊断,包括冠状动脉瘘和肺血管系统的解剖信息。后2例患者做到了这一点。在最后1例患者中,超声心动图成为诊断这种罕见畸形的重要工具,并有助于选择性心血管造影。所有4例患者均通过闭合瘘管、闭合其他主肺动脉连接以及在右心室和肺动脉之间插入带瓣管道成功进行了手术。3例患者用补片闭合了室间隔缺损。鉴于手术时已存在肺动脉高压且肺动脉系统可能不足,在其余患者的室间隔缺损处插入了带孔补片。