Ochiai Yoshie, Joo Kunihiko, Onzuka Tatsushi, Nakashima Atsuhiro, Nagatomo Yusaku, Watanabe Mamie, Muneuchi Jun
Department of Cardiovascular Surgery, Japan Community Healthcare Organization (JCHO), Kyusyu Hospital, Kitakyushu, Japan.
Department of Cardiovascular Surgery, Japan Community Healthcare Organization (JCHO), Kyusyu Hospital, Kitakyushu, Japan.
Ann Thorac Surg. 2016 Oct;102(4):e321-3. doi: 10.1016/j.athoracsur.2016.02.067.
We present a very rare case of bilateral ductus arteriosus in transposition of the great arteries with right aortic arch and aberrant retroesophageal left subclavian artery (SCA). Around 1 month after the successful arterial switch operation, the baby showed wheezing and retractive breathing. The computed tomography revealed that trachea and esophagus were sandwiched between the posterior displaced ascending aorta and the origin of the retroesophageal aberrant left SCA, the so-called Kommerell diverticulum (KD). This compression was successfully relieved by resection of the KD and division of the retroesophageal aberrant SCA through right thoracotomy.
我们报告了一例极为罕见的病例,该病例为大动脉转位合并右位主动脉弓及食管后左锁骨下动脉(SCA)异常时出现双侧动脉导管。在成功进行动脉调转手术后约1个月,婴儿出现喘息和吸气性呼吸困难。计算机断层扫描显示,气管和食管夹在向后移位的升主动脉与食管后异常左SCA的起始部之间,即所谓的Kommerell憩室(KD)。通过右胸切口切除KD并切断食管后异常SCA,成功解除了这种压迫。