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2016 Comprehensive Update of the Banff Working Group on Liver Allograft Pathology: Introduction of Antibody-Mediated Rejection.

Anthony J. Demetris, +76 more
TL;DR: New recommendations for complement component 4d tissue staining and interpretation, staging liver allograft fibrosis, and findings related to immunosuppression minimization are included.
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Origin of neointimal endothelium and alpha-actin-positive smooth muscle cells in transplant arteriosclerosis.

TL;DR: It is proposed that, although it progresses beyond the needs of functional repair, TA reflects the activity of a normal healing process that restores vascular wall function following allograft-induced immunological injury.
Journal ArticleDOI

Liver biopsy interpretation for causes of late liver allograft dysfunction

Anthony J. Demetris
- 01 Aug 2006 - 
TL;DR: The Banff Working Group on Liver Allograft Pathology herein proposes a set of consensus criteria for the most common and problematic causes of late liver allograft dysfunction, including late-onset acute and chronic rejection, recurrent and new‐onset viral and autoimmune hepatitis, biliary strictures, and recurrent primary biliary cirrhosis and primary sclerosing cholangitis.
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Pediatric liver transplantation.

TL;DR: The state-of-the-art in pediatric liver transplantation is described, with prevention of immunosuppression-related complications and promotion of as normal growth as possible.
References
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Primary biliary cirrhosis.

TL;DR: Mise a jour: anatomopathologie, anomalies immunologiques et pathogenese, tests de laboratoire, manifestations cliniques et troubles associes, evolution, traitement.
Journal ArticleDOI

Cell migration, chimerism, and graft acceptance

TL;DR: The chimeric nature of the transplanted liver was first shown in long-surviving human recipients of orthotopic hepatic allografts in 1969 and its continued presence was confirmed by the acquisition and maintenance in recipient blood of new donor-specific immunoglobulin (Gm) types and red-blood-cell alloantibodies.
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Fk 506 for liver, kidney, and pancreas transplantation

TL;DR: FK 506 was given for immunosuppression in 14 liver recipients and 2 of the 14 Liver recipients were given cadaveric kidneys, either from the same donor or from a different donor, and a third was given a pancreas as well as a kidney from the liver donor.
Journal ArticleDOI

Rethinking chronic allograft nephropathy: the concept of accelerated senescence.

TL;DR: A model in which the cumulative burden of injury and age exhausts the ability of key cells in epithelium or endothelium to repair and remodel to maintain tissue integrity is proposed, calling this exhaustion “senescence” to emphasize the importance of donor aging and the overlap of the pathologic lesions with age-related changes.
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