Hagel K J, Bommersheim H, Rautenburg H W
Z Kardiol. 1986 Mar;75(3):182-5.
Two children with cervical aortic arch are presented. This anomaly is very rare. In one patient cervical aortic arch Type A (Haughton) was associated with a ventricular septal defect and patent ductus arteriosus. In the other child we report the only case of cervical aortic arch (Type B) in association with partial anomalous pulmonary venous return.
本文报告了两名患有颈主动脉弓的儿童。这种异常非常罕见。其中一名患者的A型（霍顿型）颈主动脉弓合并室间隔缺损和动脉导管未闭。在另一名儿童中，我们报告了唯一一例B型颈主动脉弓合并部分性肺静脉异位引流的病例。
