Publication in refereed journal
香港中文大学研究人员 ( 现职)
| 赖宝山教授 (外科学系) |
| 宋银子教授 (医学院) |
全文
| 数位物件识别号 (DOI) http://dx.doi.org/10.1016/j.transproceed.2007.02.095 |
引用次数
Web of Sciencehttp://aims.cuhk.edu.hk/converis/portal/Publication/2WOS source URL
其它资讯
摘要Budd-Chiari syndrome (BCS) is one of the uncommon complications of hepatic venous reconstruction in liver transplantation. Protein-losing enteropathy (PLE) secondary to this event has rarely been described. A 14-year-old girl suffering from acute hepatic failure underwent an emergency living-related liver transplantation and developed BCS 1 year later. Her condition has been managed with several sessions of hepatic venoplasty. On one occasion, she suffered septicemia and severe diarrhea, passing large amount of fibrinoid material. The diagnosis of PLE was made clinically, which resolved immediately after reestablishment of hepatic venous patency by balloon venoplasty. This observation suggested that BCS was responsible for PLE in this patient. Prompt diagnosis and early intervention for this life-threatening condition is essential.
着者Wong J, Sin NC, Sung R, Lee PSF, Lee KF, Lai PBS
期刊名称Transplantation Proceedings
出版年份http://aims.cuhk.edu.hk/converis/portal/Publication/2007
月份6
日期1
卷号39
期次5
出版社ELSEVIER SCIENCE INC
页次1554 - 1557
国际标準期刊号0041-1345
语言英式英语
Web of Science 学科类别Immunology; IMMUNOLOGY; Surgery; SURGERY; Transplantation; TRANSPLANTATION
