Asonuma K, Shapiro A M, Inomata Y, Uryuhara K, Uemoto S, Tanaka K
Department of Transplantation and Immunology, Kyoto University, Shogoin, Japan.
Transplantation. 1999 Nov 27;68(10):1610-2. doi: 10.1097/00007890-199911270-00031.
The presence of a left-sided gallbladder poses a unique challenge for living related liver donation. Associated anomalies include segment IV atrophy, absence of portal vein bifurcation, and abnormal intrahepatic portal branches to segments II and III. The complex is rare, but is more frequent in Japan. Of 379 living related liver transplants from our institution, the complex has been encountered on four occasions (incidence: 1.1%), and we herein review our experience. Anomalies were identified preoperatively (by computed tomography and ultrasound) in all instances. One donor was turned down because there was no common portal trunk to segment II and III branches. Three donors underwent successful retrieval using a modified technique. There were no complications in the donors or recipients relating to the complex. Thus, living related liver retrieval can be achieved safely in the presence of the left-sided gallbladder/portal anomaly complex, but technical modifications are required.
左侧胆囊的存在给活体亲属肝移植带来了独特的挑战。相关异常包括肝段IV萎缩、门静脉分支缺如以及至肝段II和III的肝内门静脉分支异常。这种复合体很罕见,但在日本更为常见。在我们机构进行的379例活体亲属肝移植中,这种复合体出现过4次(发生率:1.1%),在此我们回顾我们的经验。所有病例术前均通过计算机断层扫描和超声识别出异常。一名供者被拒绝,因为肝段II和III分支没有共同的门静脉主干。三名供者采用改良技术成功进行了肝脏切取。供者或受者均未出现与该复合体相关的并发症。因此,在存在左侧胆囊/门静脉异常复合体的情况下,活体亲属肝切取可以安全完成,但需要技术改良。