Volume 13, Issue 1 pp. 150-157
Original Article
Free Access

Hepatic histological findings after transplantation for chronic hepatitis B virus infection, including a unique pattern of fibrosing cholestatic hepatitis

Susan E. Davies

Susan E. Davies

Department of Morbid Anatomy, King's College School of Medicine and Dentistry, Denmark Hill, London SE5 8RX, United Kingdom

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Bernard C. Portmann

Bernard C. Portmann

Liver Unit, King's College School of Medicine and Dentistry, Denmark Hill, London SE5 8RX, United Kingdom

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John G. O′grady

John G. O′grady

Liver Unit, King's College School of Medicine and Dentistry, Denmark Hill, London SE5 8RX, United Kingdom

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Peter M. Aldis

Peter M. Aldis

Liver Unit, King's College School of Medicine and Dentistry, Denmark Hill, London SE5 8RX, United Kingdom

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Kanchan Chaggar

Kanchan Chaggar

Liver Unit, King's College School of Medicine and Dentistry, Denmark Hill, London SE5 8RX, United Kingdom

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Graeme J. M. Alexander

Graeme J. M. Alexander

Liver Unit, King's College School of Medicine and Dentistry, Denmark Hill, London SE5 8RX, United Kingdom

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Dr. Roger Williams

Corresponding Author

Dr. Roger Williams

Liver Unit, King's College School of Medicine and Dentistry, Denmark Hill, London SE5 8RX, United Kingdom

Liver Unit, King's College Hospital, London SE5 9RS, United Kingdom===Search for more papers by this author
First published: January 1991
Citations: 409

Abstract

Long-term follow-up of 27 patients with hepatitis B virus—related chronic liver disease treated by transplantation showed that 23 had hepatitis B virus recurrence. In 13 patients late changes in the grafts were similar to those described in other series: minor abnormalities in five cases, chronic active hepatitis in five cases and non-hepatitis B virus—related graft dysfunction in three cases. Three patients had incomplete histological follow-up. Analysis of the histological changes and viral antigen expression in six cases revealed a distinct and novel pattern termed fibrosing cholestatic hepatitis. Development of fibrosing cholestatic hepatitis was associated with rapidly progressive graft dysfunction. It is postulated that this pattern of fibrosing cholestatic hepatitis develops because of a high cytoplasmic expression of viral antigens, including HBsAg. The remaining case had some features of fibrosing cholestatic hepatitis. The main histological features of this unique syndrome include thin, perisinusoidal bands of fibrosis extending from portal tracts to surround plates of ductular-type epithelium; prominent cholestasis; ground-glass transformation; and ballooning of hepatocytes with cell loss and mild mixed inflammatory reaction. (HEPATOLOGY 1991;13:150–157).

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