先天性右肺叶间肺动脉缺如：高分辨率CT表现

Congenital absence of the right interlobar pulmonary artery: HRCT findings.

作者信息

Ryu Dae Shick, Ahn Jae Hong, Choi Soo Jung, Lee Jong-hyek, Jung Seung Mun, Park Man Soo, Jung Bok-hyeon

机构信息

Department of Radiology, Gangneung Asan Hospital, College of Medicine, University of Ulsan, Gangwon-do, South Korea.

出版信息

J Thorac Imaging. 2008 Nov;23(4):292-4. doi: 10.1097/RTI.0b013e31818026db.

DOI:10.1097/RTI.0b013e31818026db

PMID:19204478

Abstract

We report a case of unilateral idiopathic pulmonary fibrosis-like changes in the right middle and lower lobe without lung volume changes and with normal upper lobe owing to congenital absence of the right interlobar pulmonary artery on chest computed tomography.

摘要

我们报告一例因胸部计算机断层扫描显示右叶间肺动脉先天性缺如，导致右中、下叶出现单侧特发性肺纤维化样改变，肺容积无变化且上叶正常的病例。