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Hepatic Complications of Hematopoietic Cell Transplantation

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Abstract

In no other medical situation is a patient at risk for so many liver diseases as during a hematopoietic cell transplant (HCT). The preparation for transplant includes either liver-toxic myeloablative therapy or intense immunosuppression that allows host microchimerism with allogeneic donor hemaotpoietic cells. As a result, patients are profoundly immunosuppressed until engraftment of infused hematopoietic stem cells; full recovery of immune function is often delayed for a year or longer; and infection with viruses, fungi, and bacteria is common. Recipients of allogeneic stem cells are also at risk for graft-versus-host disease (GVHD) involving the liver, and some patients who have received autologous or syngeneic stem cells may also develop bile duct injury resembling GVHD. Thus, a patient undergoing transplant is at risk for toxic, infectious, and immunologic liver injury. Jaundice after transplant is an ominous prognostic sign, with total serum bilirubin in the 4 to 7 mg/dL range conferring 50% mortality and bilirubin values more than 10 mg/dL conferring more than 70% mortality at d 200 posttransplant (1). Fortunately, the incidence of serious liver injury following transplant has fallen dramatically over the last decade, for several reasons.

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Shulman, H.M., McDonald, G.B. (2007). Hepatic Complications of Hematopoietic Cell Transplantation. In: Gershwin, M.E., Vierling, J.M., Manns, M.P. (eds) Liver Immunology. Humana Press. https://doi.org/10.1007/978-1-59745-518-3_32

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