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dc.rights.licenseopenen_US
hal.structure.identifierAP-HP - Hôpital Bichat - Claude Bernard [Paris]
dc.contributor.authorPOTE, Nicolas
dc.contributor.authorCARUSO, Stefano
dc.contributor.authorCADERARO, Julien
dc.contributor.authorCAUCHY, François
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorLAGADEC, Floriane
dc.contributor.authorCOUCHY, Gabrielle
dc.contributor.authorRAFFENNE, Jerome
hal.structure.identifierHôpital Henri Mondor
dc.contributor.authorAUGUSTIN, Jeremy
dc.contributor.authorVERNUCCIO, Federica
hal.structure.identifierCentre de recherche sur l'Inflammation [CRI (UMR_S_1149 / ERL_8252 / U1149)]
dc.contributor.authorVILGRAIN, Valerie
hal.structure.identifierAP-HP - Hôpital Bichat - Claude Bernard [Paris]
dc.contributor.authorHERCENT, Agathe
hal.structure.identifierAP-HP - Hôpital Bichat - Claude Bernard [Paris]
dc.contributor.authorTHEOU-ANTON, Nathalie
dc.contributor.authorZUCMAN-ROSSI, Jessica
hal.structure.identifierHôpital Beaujon [AP-HP]
dc.contributor.authorPARADIS, Valerie
dc.date.accessioned2023-12-01T08:46:48Z
dc.date.available2023-12-01T08:46:48Z
dc.date.issued2023-09-01
dc.identifier.issn1530-0285en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/186294
dc.description.abstractEnBorderline hepatocellular adenomas (BL-HCA) are characterized by focal architectural/cytologic atypia and reticulin loss, features that are insufficient for a definitive diagnosis of hepatocellular carcinoma (HCC). The diagnosis and management of BL-HCA are challenging as their biological behavior, especially in terms of malignant potential, is still debated. We aimed to compare the clinicopathologic and molecular features of BL-HCA with those of typical HCA (T-HCA), HCA with malignant transformation (HCC on HCA), and HCC to assess the risk of malignancy. One hundred six liver resection specimens were retrospectively selected from 2 reference centers, including 39 BL-HCA, 42 T-HCA, 12 HCC on HCA, and 13 HCC specimens. Somatic mutations, including TERT promoter mutations associated with HCA malignant transformation and the gene expression levels of 96 genes, were investigated in 93 frozen samples. Additionally, TERT promoter mutations were investigated in 44 formalin-fixed, paraffin-embedded samples. The clinical features of patients with BL-HCA were similar to those of patients with T-HCA, patients being mainly women (69%) with a median age of 37 years. The median tumor size was 7.5 cm, 64% of patients had a single nodule, and no recurrence was observed. Compared with T-HCA, BL-HCA was significantly enriched in β-catenin-mutated HCA in exon 3 (41% vs 6%; P < .001). Unsupervised statistical analysis based on gene expression showed that BL-HCA overlapped with T-HCA and HCC on HCA, favoring a molecular continuum of the tumors. TERT promoter mutations were observed only in HCC on HCA (42%) and in HCC (38%). In conclusion, these results suggest that despite their worrisome morphologic features, the clinicopathologic and molecular features of BL-HCA are much closer to those of T-HCA than those of HCC on HCA or HCC. This strongly supports the usefulness of combining morphologic and molecular analyses in a practical diagnostic approach for guiding the management of BL-HCA.
dc.language.isoENen_US
dc.subject.enHumans
dc.subject.enFemale
dc.subject.enAdult
dc.subject.enMale
dc.subject.enAdenoma
dc.subject.enLiver Cell
dc.subject.enCarcinoma
dc.subject.enHepatocellular
dc.subject.enLiver Neoplasms
dc.subject.enRetrospective Studies
dc.subject.enHepatectomy
dc.subject.enCell Transformation
dc.subject.enNeoplastic
dc.title.enBorderline Hepatocellular Adenomas: A Practical Diagnostic Approach Based on Pathologic and Molecular Features.
dc.title.alternativeMod Patholen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1016/j.modpat.2023.100211en_US
dc.subject.halSciences du Vivant [q-bio]/Microbiologie et Parasitologieen_US
dc.identifier.pubmed37169258en_US
bordeaux.journalModern Pathologyen_US
bordeaux.page100211en_US
bordeaux.volume36en_US
bordeaux.hal.laboratoriesMFP (Laboratoire Microbiologie Fondamentale et Pathogénicité) - UMR 5234en_US
bordeaux.issue9en_US
bordeaux.institutionCNRSen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcepubmed
hal.popularnonen_US
hal.audienceInternationaleen_US
hal.exportfalse
workflow.import.sourcepubmed
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&amp;rft_val_fmt=info:ofi/fmt:kev:mtx:journal&amp;rft.jtitle=Modern%20Pathology&amp;rft.date=2023-09-01&amp;rft.volume=36&amp;rft.issue=9&amp;rft.spage=100211&amp;rft.epage=100211&amp;rft.eissn=1530-0285&amp;rft.issn=1530-0285&amp;rft.au=POTE,%20Nicolas&amp;CARUSO,%20Stefano&amp;CADERARO,%20Julien&amp;CAUCHY,%20Fran%C3%A7ois&amp;LAGADEC,%20Floriane&amp;rft.genre=article


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