PMID- 21097715 OWN - NLM STAT- MEDLINE DCOM- 20111020 LR - 20220311 IS - 1544-2217 (Electronic) IS - 0300-9858 (Linking) VI - 48 IP - 3 DP - 2011 May TI - Histopathologic features, immunophenotyping, clonality, and eubacterial fluorescence in situ hybridization in cats with lymphocytic cholangitis/cholangiohepatitis. PG - 627-41 LID - 10.1177/0300985810384409 [doi] AB - Feline lymphocytic cholangitis is a poorly characterized disease complex with respect to histologic lesions, immunophenotype, and etiopathogenesis. Seventy-eight cases of feline lymphocytic cholangitis (n = 51) and feline hepatic lymphoma (n = 27) were reviewed using standardized histopathology, immunophenotyping (B cell and T cell), polymerase chain reaction for T-cell receptor (TCR) gene rearrangement, and fluorescence in situ hybridization (FISH) for eubacteria. Five histopathologic features in cases of lymphocytic cholangitis assisted in its differentiation from hepatic lymphoma: bile duct targeting (n = 32, 62.7%), ductopenia (n = 9, 17.6%), peribiliary fibrosis (n = 37, 72.5%), portal B-cell aggregates (n = 36, 70.6%), and portal lipogranulomas (n = 38, 74.5%). The majority of lymphocytic cholangitis cases (n = 35, 68.6%) were T cell predominant; 15 (29.4%) had an equal mix of B cells and T cells, and 1 (1.9%) had a B cell-predominant infiltrate; 66.6% of hepatic lymphoma cases were T-cell lymphomas. TCR clonality results were unexpected, with 17.1% of cases of lymphocytic cholangitis having clonal or oligoclonal populations and with T-cell lymphomas having variable TCR clonality (63.6% clonal or oligoclonal, 36.3% polyclonal). The majority of lymphocytic cholangitis (n = 32 of 36, 88.8%) and all hepatic lymphoma cases had no detectable eubacteria using FISH. As demonstrated here, bile duct targeting, ductopenia, peribiliary fibrosis, portal B-cell aggregates, and portal lipogranulomas are lymphocytic cholangitis features that, along with polyclonal TCR (83%), help differentiate it from hepatic lymphoma. No strong evidence was found implicating in situ bacterial colonization as an etiopathogenesis of lymphocytic cholangitis. FAU - Warren, A AU - Warren A AD - Department of Veterinary Clinical and Diagnostic Sciences, University of Calgary, Calgary, Canada. alwarren@ucalgary.ca FAU - Center, S AU - Center S FAU - McDonough, S AU - McDonough S FAU - Chiotti, R AU - Chiotti R FAU - Goldstein, R AU - Goldstein R FAU - Meseck, E AU - Meseck E FAU - Jacobsen, M AU - Jacobsen M FAU - Rowland, P AU - Rowland P FAU - Simpson, K AU - Simpson K LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20101119 PL - United States TA - Vet Pathol JT - Veterinary pathology JID - 0312020 SB - IM MH - Animals MH - Cat Diseases/genetics/microbiology/*pathology MH - Cats MH - Cholangitis/genetics/pathology/*veterinary MH - Female MH - Genetic Predisposition to Disease MH - Hepatitis, Animal/genetics/*pathology MH - Immunohistochemistry/veterinary MH - Immunophenotyping/*veterinary MH - Liver/pathology MH - Male MH - Polymerase Chain Reaction MH - Retrospective Studies EDAT- 2010/11/26 06:00 MHDA- 2011/10/21 06:00 CRDT- 2010/11/25 06:00 PHST- 2010/11/25 06:00 [entrez] PHST- 2010/11/26 06:00 [pubmed] PHST- 2011/10/21 06:00 [medline] AID - 0300985810384409 [pii] AID - 10.1177/0300985810384409 [doi] PST - ppublish SO - Vet Pathol. 2011 May;48(3):627-41. doi: 10.1177/0300985810384409. Epub 2010 Nov 19.