双主动脉弓伴右主动脉弓发育不全及左主动脉弓C型闭锁。
Double aortic arch with hypoplastic right aortic arch and type C atresia of left aortic arch.
作者信息
Costanzo Luca, Caruso Elio, Agati Salvatore, Guccione Paolo
机构信息
Department of Pediatric Cardiology and Cardiac Surgery, Bambino Gesù Children's Hospital Centro Cardiologico Pediatrico del Mediterraneo, San Vincenzo Hospital, Taormina, Italy.
Department of Pediatric Cardiology and Cardiac Surgery, Bambino Gesù Children's Hospital Centro Cardiologico Pediatrico del Mediterraneo, San Vincenzo Hospital, Taormina, Italy
出版信息
Interact Cardiovasc Thorac Surg. 2014 Aug;19(2):331-3. doi: 10.1093/icvts/ivu147. Epub 2014 May 15.
We report the case of a 2-month-old baby with a double aortic arch, type C atresia of the left arch and severe hypoplasia of the right aortic arch between the right carotid and subclavian arteries, resulting in systemic obstruction, left ventricular dysfunction and congestive heart failure. Surgical augmentation of the right aortic arch ameliorated the obstruction with improvement in left ventricular function and symptoms.
我们报告了一例2个月大婴儿的病例，该婴儿患有双主动脉弓，左弓C型闭锁，右主动脉弓在右颈动脉和锁骨下动脉之间严重发育不全，导致全身梗阻、左心室功能障碍和充血性心力衰竭。对右主动脉弓进行手术扩大改善了梗阻情况，左心室功能和症状也有所改善。
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