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Fulminant hepatitis B virus: Recurrence after liver transplantation in two patients also infected with hepatitis delta virus

  • Willem A. Marsman
  • , Russell H. Wiesner
  • , Kenneth P. Batts
  • , John J. Poterucha
  • , Michael K. Porayko
  • , Hubert G.M. Niesters
  • , Pieter E. Zondervan
  • , Ruud A.F. Krom

Research output: Contribution to journal › Article › peer-review

Abstract

Liver transplantation for hepatitis B virus (HBV)-related liver disease is complicated by HBV recurrence and, consequently, poor patient and graft survival. Patients transplanted for hepatitis delta virus (HDV)-related cirrhosis are reported to have a diminished incidence of HBV recurrence and improved graft survival. However, only a few reported HDV-infected patients had active HBV replicative disease before liver transplantation. In our experience, we transplanted two HDV-infected patients, both of whom had active HBV replication before liver transplantation. In one patient, hepatitis B surface antigen (HBsAg) recurred four months after transplantation. Two months later, Hepatitis Be antigen (HBeAg) and HBV-DNA became positive, and the patient died of fulminant recurrent hepatitis B and hepatitis delta. In the other patient, HBV persisted after transplantation, and 2 months later the patient required retransplantation for fulminant recurrent hepatitis B and hepatitis delta. With the second graft, the patient remained free of HBV infection for 1 year. Thereafter, the patient experienced HBV recurrence with active replication and died of fulminant hepatitis B and delta recurrence. In the first ease and in the second graft of the second case, hepatitis B immunoglobulin (HBIG) immunoprophylaxis was administered in an attempt to prevent recurrence of HBV. The literature suggests that an HDV infection inhibits the replication of HBV and therefore plays a role in preventing the recurrence of HBV and improving survival. Our experience with two patients suggests that HDV infection, in the presence of active HBV replication, may not play a protective role.

Original languageEnglish (US)
Pages (from-to)434-438
Number of pages5
JournalHepatology
Volume25
Issue number2
DOIs
StatePublished - Feb 1997

ASJC Scopus subject areas

  • Hepatology

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