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J Clin Pathol 2010;63:47-74 doi:10.1136/jcp.2009.068254
  • My approach

Liver allograft pathology: approach to interpretation of needle biopsies with clinicopathological correlation

  1. O Adeyi,
  2. S E Fischer,
  3. M Guindi
  1. Laboratory Medicine Program, University Health Network/University of Toronto, Toronto, Ontario, Canada
  1. Correspondence to Maha Guindi, Laboratory Medicine Program, University Health Network/University of Toronto, 200 Elizabeth Street, Eaton 11-444, Toronto, Ontario, Canada M5G 2C4; maha.guindi{at}uhn.on.ca
  • Accepted 1 October 2009
  • Published Online First 21 October 2009

Abstract

The spectrum of diseases encountered in post-transplant liver pathology biopsies is broad. In this review, these have been divided as belonging to one of three categories: (1) new-onset/de novo post-transplant abnormalities (early and late), (2) rejection, and (3) recurrence of original disease. The clinical and pathological features of the entities making up each category, with the relevant differential diagnosis and overlaps between and within these groups, are discussed and illustrated. Recurrent or de novo neoplasms make up a fourth category not included in this review. Early new-onset conditions are mostly related to surgical complications, donor factors and ischaemia to the graft. These include reperfusion/preservation injury, lipopeliosis, small-for-size-syndrome, biliary sludge syndrome and hepatic artery thrombosis. The various forms of rejection (cellular, chronic, antibody-mediated, and late atypical rejection) are detailed. Most chronic liver diseases can and do recur in the graft. They may display features that overlap with de novo conditions (eg, primary sclerosing cholangitis versus chronic rejection). As with most cases of allograft biopsy interpretation, accurate diagnosis rests with careful correlation of histological features with clinical, imaging and laboratory findings, and often comparison with previous sequential and follow-up biopsies. Late-onset new diseases include biliary strictures, idiopathic chronic hepatitis and de novo autoimmune hepatitis, among others. This review provides a practical approach to the interpretation of these challenging biopsies. Selected difficult scenarios or conundrums are identified and discussed in the relevant sections.

Footnotes

  • Competing interests None.

  • Provenance and Peer review Commissioned; not externally peer reviewed.

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