Internal Ileal Diversion as Treatment for Progressive Familial Intrahepatic Cholestasis Type 1-Associated Graft Inflammation and Steatosis after Liver Transplantation

Background: Progressive Familial Intrahepatic cholestasis type I (PFIC1) is a rare congenital hepatopathy causing cholestasis with progressive liver disease. Surgical interruption of the enterohepatic circulation, e.g., surgical biliary diversion (SBD) can slow down development of liver cirrhosis. E...

Full description

Saved in:
Bibliographic Details
Main Authors: Anna M. Kavallar (Author), Franka Messner (Author), Stefan Scheidl (Author), Rupert Oberhuber (Author), Stefan Schneeberger (Author), Denise Aldrian (Author), Valeria Berchtold (Author), Murat Sanal (Author), Andreas Entenmann (Author), Simon Straub (Author), Anna Gasser (Author), Andreas R. Janecke (Author), Thomas Müller (Author), Georg F. Vogel (Author)
Format: Book
Published: MDPI AG, 2022-12-01T00:00:00Z.
Subjects:
Online Access:Connect to this object online.
Tags: Add Tag
No Tags, Be the first to tag this record!

MARC

LEADER 00000 am a22000003u 4500
001 doaj_3f6935a47f1e4c8bb488a1303a8fa774
042 |a dc 
100 1 0 |a Anna M. Kavallar  |e author 
700 1 0 |a Franka Messner  |e author 
700 1 0 |a Stefan Scheidl  |e author 
700 1 0 |a Rupert Oberhuber  |e author 
700 1 0 |a Stefan Schneeberger  |e author 
700 1 0 |a Denise Aldrian  |e author 
700 1 0 |a Valeria Berchtold  |e author 
700 1 0 |a Murat Sanal  |e author 
700 1 0 |a Andreas Entenmann  |e author 
700 1 0 |a Simon Straub  |e author 
700 1 0 |a Anna Gasser  |e author 
700 1 0 |a Andreas R. Janecke  |e author 
700 1 0 |a Thomas Müller  |e author 
700 1 0 |a Georg F. Vogel  |e author 
245 0 0 |a Internal Ileal Diversion as Treatment for Progressive Familial Intrahepatic Cholestasis Type 1-Associated Graft Inflammation and Steatosis after Liver Transplantation 
260 |b MDPI AG,   |c 2022-12-01T00:00:00Z. 
500 |a 10.3390/children9121964 
500 |a 2227-9067 
520 |a Background: Progressive Familial Intrahepatic cholestasis type I (PFIC1) is a rare congenital hepatopathy causing cholestasis with progressive liver disease. Surgical interruption of the enterohepatic circulation, e.g., surgical biliary diversion (SBD) can slow down development of liver cirrhosis. Eventually, end stage liver disease necessitates liver transplantation (LT). PFIC1 patients might develop diarrhea, graft steatosis and inflammation after LT. SBD after LT was shown to be effective in the alleviation of liver steatosis and graft injury. Case report: Three PFIC1 patients received LT at the ages of two, two and a half and five years. Shortly after LT diarrhea and graft steatosis was recognized, SBD to the terminal ileum was opted to prevent risk for ascending cholangitis. After SBD, inflammation and steatosis was found to be reduced to resolved, as seen by liver biochemistry and ultrasounds. Diarrhea was reported unchanged. Conclusion: We present three PFIC1 cases for whom SBD to the terminal ileum successfully helped to resolve graft inflammation and steatosis. 
546 |a EN 
690 |a PFIC1 
690 |a pediatric liver transplantation 
690 |a steatosis 
690 |a surgical biliary diversion 
690 |a Pediatrics 
690 |a RJ1-570 
655 7 |a article  |2 local 
786 0 |n Children, Vol 9, Iss 12, p 1964 (2022) 
787 0 |n https://www.mdpi.com/2227-9067/9/12/1964 
787 0 |n https://doaj.org/toc/2227-9067 
856 4 1 |u https://doaj.org/article/3f6935a47f1e4c8bb488a1303a8fa774  |z Connect to this object online.