Elseidy Sheref A, Awad Ahmed K, Zamani Zarlakhta, Khaurana Shryia, Mohamad Tamam
Department of Cardiovascular Diseases, Ain Shams University Hospitals, Cairo, Egypt.
Department of Cardiovascular Surgery, Ain Shams University Hospitals, Cairo, Egypt.
Indian J Thorac Cardiovasc Surg. 2022 Jul;38(4):408-411. doi: 10.1007/s12055-021-01286-y. Epub 2022 Jan 27.
Right aortic arch (RAA) with an aberrant left subclavian artery (LSA) is a very rare anatomical variant of the aorta, which is rarely symptomatic. However, symptoms may vary depending on the relationship of the aberrant subclavian artery to the surrounding structures. In this report, we present a case of an 8-year-old girl who was identified with Edward's type II RAA with LSA after developing a list of symptoms that led to the diagnosis of pulmonary sequestration, which in turn led to the discovery of her congenital aortic abnormality.
右位主动脉弓（RAA）伴迷走左锁骨下动脉（LSA）是一种非常罕见的主动脉解剖变异，很少有症状。然而，症状可能因迷走锁骨下动脉与周围结构的关系而异。在本报告中，我们介绍了一名8岁女孩的病例，她在出现一系列症状后被诊断为伴有LSA的爱德华氏II型RAA，这些症状导致了肺隔离症的诊断，进而发现了她的先天性主动脉异常。
