Yon James R, Ravenel James G
Department of Radiology and Radiologic Science, Medical University of South Carolina, Charleston, SC 29425, USA.
J Comput Assist Tomogr. 2010 May-Jun;34(3):418-20. doi: 10.1097/RCT.0b013e3181d1e96e.
We report the case of a 21-year-old man who presented with a hilar mass and whose condition was diagnosed as a congenital anomalous communication between the bronchial and pulmonary artery. We review his lung vascular embryology and anatomy that led to this rare systemic to pulmonary arterial shunt, describe other etiologies that may lead to abnormal systemic artery to pulmonary artery communication, and briefly discuss treatment options.
我们报告了一例21岁男性病例,该患者表现为肺门肿块,其病情被诊断为支气管与肺动脉之间的先天性异常交通。我们回顾了导致这种罕见的体循环至肺动脉分流的肺血管胚胎学和解剖学知识,描述了可能导致异常体动脉至肺动脉交通的其他病因,并简要讨论了治疗方案。