Chawla Soni C, Jha Priyanka, Breiman Richard, Farmer Diana, Gooding Charles
Department of Radiological Sciences, Olive View-UCLA Medical Center, 14445 Olive View Drive, Sylmar, CA 91342, USA.
Pediatr Radiol. 2008 Sep;38(9):999-1002. doi: 10.1007/s00247-008-0880-3. Epub 2008 May 14.
Congenital tracheobiliary fistula (CTBF) is a rare malformation. So far 24 cases have been reported in the English language literature. The imaging techniques used in diagnosis have been bronchography, fistulography, cholangiography, hepatobiliary nuclear imaging and MRI. We report a newborn patient who presented with right lung consolidation and biliptysis. The radiographic diagnosis of tracheobiliary fistula was made on multidetector CT scan of the chest and abdomen. Multiple 3-D volume-rendered reformations were performed. An abnormal air-filled tract was seen connecting the posteroinferior aspect of the carina and left biliary system, which was successfully treated surgically.
先天性气管胆管瘘(CTBF)是一种罕见的畸形。迄今为止,英文文献中已报道了24例。诊断中使用的成像技术包括支气管造影、瘘管造影、胆管造影、肝胆核素成像和MRI。我们报告了一名出现右肺实变和胆汁咳出的新生儿患者。通过胸部和腹部的多排螺旋CT扫描做出了气管胆管瘘的影像学诊断。进行了多次三维容积再现重建。可见一条异常的充气通道连接隆突后下部和左胆道系统,该患者通过手术成功治愈。