Semiz-Oysu Aslihan, Basaran Ipek, Barutca Hakan, Bukte Yasar
Department of Radiology, Umraniye Training and Research Hospital, Ümraniye Eğitim ve Araştırma Hastanesi, Adem Yavuz Cad. No: 1, Ümraniye, Istanbul, 34766, Turkey,
Pediatr Cardiol. 2013;34(8):1928-31. doi: 10.1007/s00246-012-0463-9. Epub 2012 Aug 11.
A case of aberrant left pulmonary artery originating from the right pulmonary artery resembling pulmonary artery sling malformation, but without true sling formation, is presented. Anomalous left pulmonary artery was accompanied with long-segment proximal tracheal stenosis and other congenital malformations typically associated with PAS complex. The anomalous pulmonary artery passed anterior to the trachea; therefore, no true sling was formed. Because no airway compression by the aberrant left pulmonary artery was detected, the proximal tracheal stenosis was thought to be primary.
本文报告一例起源于右肺动脉的异常左肺动脉,形似肺动脉吊带畸形,但未形成真正的吊带。异常左肺动脉伴有长段近端气管狭窄及其他通常与肺动脉吊带综合征相关的先天性畸形。异常肺动脉走行于气管前方,因此未形成真正的吊带。由于未检测到异常左肺动脉对气道的压迫,近端气管狭窄被认为是原发性的。