Abstract

Auxiliary grafts have a high risk of Hepatitis B virus (HBV) infection in patients with chronic HBV-related diseases. Hepatitis B virus-related auxiliary partial orthotopic liver transplantation (APOLT) cases were reviewed to show the results of current methods to block native-to-graft HBV transmission. Three patients received APOLT for HBV-related liver cirrhosis and a recurrent upper gastrointestinal hemorrhage between April 2015 and January 2017 by the liver transplant team of Beijing Friendship Hospital affiliated with Capital Medical University. All three patients were positive for HBV surface antigen (HBsAg) and had a negative HBV DNA test result before transplantation. After auxiliary transplantations, HBsAg was found to be positive in two patients and negative in one patient. To avoid graft infection of HBV, entecavir-based therapy was employed and the remnant native livers of the recipients were removed 51–878 days after liver transplantation. Then, serum conversions of HBsAg were found in all three cases. For the first time, this case series shows the possibility of blocking the transmission of HBV from a native liver to a graft in auxiliary transplantation by entecavir-based therapy. Among the cases, a left lobe graft was successfully implanted as a replacement of the right lobe of the recipient, which is also discussed.

Highlights

  • In auxiliary partial orthotopic liver transplantation (APOLT), a liver graft is implanted while the partial or entire native liver is preserved

  • All three patients recovered from the operations, and their liver functions were normal at the end of the follow-up

  • A biliary anastomotic stricture was found in patient C 391 days after transplantation, which was treated successfully by percutaneous transhepatic cholangiodrainage (PTCD)

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Summary

Introduction

In auxiliary partial orthotopic liver transplantation (APOLT), a liver graft is implanted while the partial or entire native liver is preserved. Auxiliary partial orthotopic liver transplantation is commonly used in patients with acute liver failure or metabolic liver diseases [1, 2]. Patients who receive APOLT for acute liver failure, a reversible liver disease, may be able to discontinue immunosuppressant treatment after their native liver has regenerated [3]. Some inherent liver metabolic defects can be corrected by a small auxiliary graft as a special form of gene therapy [4, 5]. Auxiliary partial orthotopic liver transplantation can be employed when a whole liver graft cannot be acquired or the graft volume is inadequate [6, 7]

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