PMID- 28618047 OWN - NLM STAT- MEDLINE DCOM- 20180723 LR - 20180723 IS - 1365-2559 (Electronic) IS - 0309-0167 (Linking) VI - 71 IP - 6 DP - 2017 Dec TI - Focal beta-catenin mutation identified on formalin-fixed and paraffin-embedded inflammatory hepatocellular adenomas. PG - 989-993 LID - 10.1111/his.13283 [doi] AB - The identification of hepatocellular adenoma (HCA) with mutation in exon 3 of the CTNNB1 gene encoding for beta-catenin is clinically relevant due to a higher risk of malignant transformation. Inflammatory HCA (IHCA) can exhibit beta-catenin activation (beta-IHCA). We report two cases with multiple IHCA in which focal beta-catenin activation has been found in one of the IHCA. In both cases, the diagnosis of IHCA was confirmed on the resected nodules by routine stains, immunohistochemical detection of C-reactive protein (CRP) and molecular biology on frozen material. An additional molecular analysis was performed on formalin-fixed paraffin-embedded (FFPE) material that showed focal glutamine synthetase (GS) staining, the surrogate marker of beta-catenin activation. In case 1, it was a 1.8-cm area within the 7.5 cm IHCA, and in case 2 a small 0.3-cm area within a 1.8 cm resected IHCA located close to a larger IHCA, negative for GS. In both cases, nuclear beta-catenin expression and decreased reticulin network were observed in the GS expressing foci, together with cholestasis and diffuse CD34 expression in case 1. Molecular analysis by pyrosequencing on FFPE material using the GS-stained slides as reference to select areas with/without positive staining revealed a CTNNB1 exon 3 mutation restricted to the areas exhibiting both positive GS and CRP expression, whereas wild-type CTNNB1 was found in areas showing only CRP staining. These two cases illustrate focal beta-catenin activation that can occur within IHCAs. Additional data are needed to determine if beta-catenin mutation is a secondary event in IHCA. CI - (c) 2017 John Wiley & Sons Ltd. FAU - Saldarriaga, Joan AU - Saldarriaga J AD - Service of Clinical Pathology, Lausanne University Hospital, Institute of Pathology, Lausanne, Switzerland. FAU - Bisig, Bettina AU - Bisig B AD - Service of Clinical Pathology, Lausanne University Hospital, Institute of Pathology, Lausanne, Switzerland. FAU - Couchy, Gabrielle AU - Couchy G AD - Functional Genomics of Solid Tumors, Universite Paris Descartes, Universite Paris Diderot, Paris, France. FAU - Castain, Claire AU - Castain C AD - Service de Pathologie, Hopital Pellegrin, CHU Bordeaux, Bordeaux, France. FAU - Zucman-Rossi, Jessica AU - Zucman-Rossi J AD - Functional Genomics of Solid Tumors, Universite Paris Descartes, Universite Paris Diderot, Paris, France. FAU - Balabaud, Charles AU - Balabaud C AD - Inserm UMR 1053, Universite Bordeaux, Bordeaux, France. FAU - Sempoux, Christine AU - Sempoux C AD - Service of Clinical Pathology, Lausanne University Hospital, Institute of Pathology, Lausanne, Switzerland. FAU - Bioulac-Sage, Paulette AU - Bioulac-Sage P AUID- ORCID: 0000-0001-5952-0623 AD - Service de Pathologie, Hopital Pellegrin, CHU Bordeaux, Bordeaux, France. AD - Inserm UMR 1053, Universite Bordeaux, Bordeaux, France. LA - eng PT - Journal Article DEP - 20171006 PL - England TA - Histopathology JT - Histopathology JID - 7704136 RN - 0 (Biomarkers, Tumor) RN - 0 (CTNNB1 protein, human) RN - 0 (beta Catenin) RN - 1HG84L3525 (Formaldehyde) RN - 9007-41-4 (C-Reactive Protein) RN - EC 6.3.1.2 (Glutamate-Ammonia Ligase) SB - IM MH - Adenoma, Liver Cell/*genetics/pathology MH - Adult MH - Biomarkers, Tumor/*genetics/metabolism MH - C-Reactive Protein/metabolism MH - Cell Transformation, Neoplastic MH - Female MH - Formaldehyde MH - Glutamate-Ammonia Ligase/metabolism MH - Humans MH - Immunohistochemistry MH - Liver Neoplasms/*genetics/pathology MH - Microdissection MH - Middle Aged MH - Mutation MH - Paraffin Embedding MH - beta Catenin/*genetics/metabolism OTO - NOTNLM OT - C-reactive protein OT - exon3 CTNNB1 mutation OT - glutamine synthetase OT - malignant transformation OT - microdissection EDAT- 2017/06/16 06:00 MHDA- 2018/07/24 06:00 CRDT- 2017/06/16 06:00 PHST- 2017/04/06 00:00 [received] PHST- 2017/06/10 00:00 [accepted] PHST- 2017/06/16 06:00 [pubmed] PHST- 2018/07/24 06:00 [medline] PHST- 2017/06/16 06:00 [entrez] AID - 10.1111/his.13283 [doi] PST - ppublish SO - Histopathology. 2017 Dec;71(6):989-993. doi: 10.1111/his.13283. Epub 2017 Oct 6.