Lawrence T Y, Stiles Q R
Am J Dis Child. 1975 Oct;129(10):1229-31. doi: 10.1001/archpedi.1975.02120470073022.
Persistence of the fifth aortic arch is a rare vascular anomaly of man, and in all cases reported thus far there has been an associated patent ductus Botalli (arteriosus). The present case is unique in at least three respects: lack of associated intracardiac malformation, the survival of the patient, and prenatal exposure to the possible teratogenic action of the anticonvulsant drug trimethadione (Tridione). Other noncardiovascular congenital defects were present in our patient. The dislocation of the hip and the patent ductus arteriosus have been corrected surgically.
第五主动脉弓持续存在是一种罕见的人类血管异常,在迄今为止报道的所有病例中,均伴有动脉导管未闭。本病例至少在三个方面具有独特性:无相关心脏内畸形、患者存活以及产前暴露于抗惊厥药物三甲双酮(曲二酮)可能的致畸作用。我们的患者还存在其他非心血管先天性缺陷。髋关节脱位和动脉导管未闭已通过手术矫正。