Kadoba K, Kawashima Y, Matsuda H, Sakakibara T, Hirose H, Sano T, Ogawa M
Pediatr Cardiol. 1987;8(2):143-6. doi: 10.1007/BF02079473.
The case of a 2-year-old boy with tetralogy of Fallot and a complete double aortic arch (both arches patent) is reported. The left dominant aortic arch ran retroesophageally to the right and joined with the right smaller arch to form the descending thoracic aorta on the right side. We employed a right thoracotomy and performed a division of the right nondominant arch at the connection with the descending aorta. The surgical implications of an unusual type of double aortic arch are discussed.
报道了一名患有法洛四联症和完全性双主动脉弓（双侧弓均通畅）的2岁男孩病例。左优势主动脉弓经食管后方走向右侧，与较小的右弓相连，在右侧形成降主动脉。我们采用右胸切开术，在右非优势弓与降主动脉连接处将其切断。讨论了这种不寻常类型双主动脉弓的手术意义。
