Pediatric Cardiology and Pediatric Interventional Cardiology Department, Universitat Autònoma Barcelona, Hospital Vall d'Hebron, Barcelona, Spain.
Pediatric Cardiology Department, Universitat de Girona, Hospital Doctor Josep Trueta, Girona, Spain.
World J Pediatr Congenit Heart Surg. 2020 Jul;11(4):NP140-NP143. doi: 10.1177/2150135117752895. Epub 2018 Apr 3.
"Persistence of the fifth aortic arch" is a rare congenital cardiovascular anomaly that consists of an abnormal vessel arising from the distal ascending aorta connecting with the systemic or pulmonary circulation. We report a case of a type A interruption of the aortic arch and a coarctation of the fifth aortic arch, which connected the ascending with the descending aorta. No cardiac surgery was required because a covered stent was successfully implanted in the fifth aortic arch when the patient was 4 years old. A chromosome 9 q arm duplication of uncertain significance was also found, an anomaly never described before in this clinical context.
“第五主动脉弓永存”是一种罕见的先天性心血管畸形,由起源于升主动脉远端的异常血管引起,与体循环或肺循环相连。我们报告了一例主动脉弓中断伴第五主动脉弓缩窄的病例,该缩窄连接了升主动脉和降主动脉。由于患者 4 岁时成功植入了覆膜支架,因此无需心脏手术。还发现了一条意义未明的 9q 臂染色体重复,这在该临床情况下以前从未描述过。