Waldman J D, Lamberti J J
Pediatric Cardiology Medical Group, Children's Hospital, San Diego, California.
Am J Cardiovasc Pathol. 1988;1(3):361-7.
In three patients with complex cyanotic congenital heart disease, the conus was found to have no arterial outlet. The semilunar valves were at similar, caudad levels, and there was malposition of the great arteries. The aorta was related to the body--not the outflow portion--of the right ventricle in two patients with transposition and to the body of the left ventricle in one child with single ventricle. These cases confirm the independent embryological segregation of the conus and the truncus. Failure to recognize this condition can lead to erroneous relationship diagnoses and may adversely influence surgical decisions.
在3例复杂紫绀型先天性心脏病患者中,发现圆锥无动脉出口。半月瓣处于相似的尾侧水平,且大动脉位置异常。在2例大动脉转位患者中,主动脉与右心室的体部而非流出道相连,在1例单心室患儿中,主动脉与左心室的体部相连。这些病例证实了圆锥和动脉干在胚胎学上是独立分离的。未能认识到这种情况可能导致错误的关系诊断,并可能对手术决策产生不利影响。