Zapata H, Edwards J E, Titus J L
Department of Pediatrics, University of Minnesota, Minneapolis.
Pediatr Cardiol. 1993 Jul;14(3):159-61. doi: 10.1007/BF00795645.
Anomalous origin of the right subclavian artery (ARSA) from the aorta distal to the normally positioned left subclavian artery is a relatively frequent congenital anomaly in subjects with left aortic arch. The purpose of this study was to determine the relative frequency of associated cardiovascular anomalies in individuals with this anomaly. From the records of approximately 11,000 pathologic specimens in the Registry of Cardiovascular Disease of United Hospital (St. Paul, MN, USA), we found 128 (1.2%) with ARSA. Of the 128 ARSA, 117 (2.9%) occurred among 4102 instances of congenital heart disease. The 117 cases with congenital heart disease and ARSA were conotruncal anomalies in 38%, septal defects in 28%, obstructive anomalies of the left side of the heart in 21%, right heart anomalies in 5%, and miscellaneous conditions in the other 8%. Down syndrome existed in 14 (12%) of the 117 specimens with ARSA and some congenital cardiac anomaly; nine of the latter had an atrioventricular canal (AVC) malformation.
右锁骨下动脉(ARSA)起源于主动脉且位于正常位置的左锁骨下动脉远端,这在左主动脉弓患者中是一种相对常见的先天性异常。本研究的目的是确定患有这种异常的个体中相关心血管异常的相对发生率。从美国明尼苏达州圣保罗联合医院心血管疾病登记处约11,000份病理标本记录中,我们发现128例(1.2%)患有ARSA。在这128例ARSA中,117例(2.9%)出现在4102例先天性心脏病病例中。117例患有先天性心脏病和ARSA的病例中,38%为圆锥动脉干异常,28%为间隔缺损,21%为心脏左侧梗阻性异常,5%为右心异常,其余8%为其他杂症。117例患有ARSA和某些先天性心脏异常的标本中有14例(12%)存在唐氏综合征;其中9例患有房室通道(AVC)畸形。