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主动脉弓中断合并主肺动脉间隔缺损。解剖学回顾。

Interruption of the aortic arch with aorticopulmonary septal defect. An anatomic review.

作者信息

Braunlin E, Peoples W M, Freedom R M, Fyler D C, Goldblatt A, Edwards J E

出版信息

Pediatr Cardiol. 1982;3(4):329-35. doi: 10.1007/BF02427036.

Abstract

Interruption of the aortic arch may occur with aorticopulmonary septal defect (APSD) as part of a developmental complex. The anatomic details of 46 cases of interruption of the aortic arch with APSD revealed the following characteristics: (1) type A interruption of the aortic arch occurred nearly six times more commonly than type B interruption; (2) the APSD was variable in size and position, conforming to the types previously described; (3) the ventricular septum was usually intact, but a ventricular septal defect was present in six cases and occurred more frequently with type B interruption of the aortic arch; (4) subaortic stenosis was not present in any of the 16 cases in which adequate details were available to make a judgment. The association of APSD with interruption of the aortic arch in infancy is not uncommon. Evaluation of infants with APSD should thus include evaluation of the aortic arch. The occurrence of interruption of the aortic arch with an intact ventricular septum is distinctly unusual. In such cases an APSD should be suspected and sought.

摘要

主动脉弓中断可能与主动脉肺动脉间隔缺损(APSD)同时出现,作为一种发育复合体的一部分。46例伴有APSD的主动脉弓中断病例的解剖学细节显示出以下特征:(1)A型主动脉弓中断的发生频率几乎是B型中断的6倍;(2)APSD的大小和位置各不相同,符合先前描述的类型;(3)室间隔通常完整,但有6例存在室间隔缺损,且在B型主动脉弓中断中更常见;(4)在16例有足够细节可供判断的病例中,均未发现主动脉瓣下狭窄。婴儿期APSD与主动脉弓中断的关联并不罕见。因此,对患有APSD的婴儿进行评估应包括对主动脉弓的评估。室间隔完整的主动脉弓中断的发生明显不常见。在这种情况下,应怀疑并寻找APSD。

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