Ermis Cengiz, Gupta-Malhotra Monesha, Titus Jack L
Division of Cardiology, University of Minnesota, Minneapolis, MN, USA.
Cardiol Young. 2004 Feb;14(1):99-101. doi: 10.1017/s1047951104001209.
As far as we are aware, a bicuspid aortic valve has not previously been reported in the setting of tetralogy of Fallot and pulmonary atresia. We describe this association in a newborn who presented with a murmur and cyanosis. Echocardiography showed tetralogy of Fallot with pulmonary atresia, and also a moderately stenotic bicuspid aortic valve. The patient underwent open-heart surgery guided by transesophageal echocardiography. Postoperatively, there was only mild obstruction across both outflow tracts. We have also reviewed the pertinent data from our Jesse E. Edwards Registry of Cardiovascular Disease to establish the incidence of bicuspid aortic valve in the setting of obstruction of the right ventricular outflow tract, finding the association in no patients with pulmonary atresia and tetralogy of Fallot, in 0.7% of those with tetralogy of Fallot and pulmonary stenosis, but in 6.6% of those with pulmonary atresia and intact ventricular septum.
据我们所知,此前尚未有关于法洛四联症合并肺动脉闭锁时出现二叶式主动脉瓣的报道。我们描述了一名出现杂音和发绀的新生儿中的这种关联情况。超声心动图显示为法洛四联症合并肺动脉闭锁,同时还有一枚中度狭窄的二叶式主动脉瓣。该患者在经食管超声心动图引导下接受了心脏直视手术。术后,两个流出道仅存在轻度梗阻。我们还查阅了我们的杰西·E·爱德华兹心血管疾病登记处的相关数据,以确定右心室流出道梗阻情况下二叶式主动脉瓣的发生率,结果发现法洛四联症合并肺动脉闭锁的患者中未发现这种关联,法洛四联症合并肺动脉狭窄的患者中有0.7%存在这种关联,但在肺动脉闭锁且室间隔完整的患者中有6.6%存在这种关联。