Evidence map›Paper›PMID 42034893›Full record

ReviewJHEP reports : innovation in hepatology2026

New histopathological terminology for well-differentiated hepatocellular lesions in unusual clinico-pathological scenarios: HCA-like and FNH-like.

Christine Sempoux, Venancio Af Alves, Johanna Arola, Charles Balabaud, Paulette Bioulac-Sage, Romano Colombari, James M Crawford, Amar P Dhillon, Luca di Tommaso, Linda D Ferrell and 17 more

Abstract readReview
In one paragraph

Review in JHEP reports : innovation in hepatology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

27 authors.

Christine SempouxInstitute of Pathology, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland. Electronic address: christine.sempoux@chuv.ch.
Venancio Af AlvesDepartment of Pathology, University of Sao Paulo School of Medicine, Sao Paulo, Brazil.
Johanna ArolaDepartment of Pathology, Helsinki University Hospital, Diagnostic Centre, and Faculty of Medicine, University of Helsinki, Helsinki, Finland.
Charles BalabaudInserm, U1053, Bordeaux University, Bordeaux, France.
Paulette Bioulac-SageInserm, U1053, Bordeaux University, Bordeaux, France.
Romano ColombariDepartment of Pathology, San Bonifacio Hospital, Verona, Italy.
James M CrawfordNorthwell Health, Department of Pathology and Laboratory Medicine, New Hyde Park, NY, USA.
Amar P DhillonDepartment of Cellular Pathology, UCL Medical School, London, UK.
Luca di TommasoPathology Unit, IRCCS Humanitas Research Hospital, and Department of Biomedical Sciences, Humanitas University, Milan, Italy.
Linda D FerrellDepartment of Pathology, University of California, San Francisco, CA, USA.
Ryan M GillDepartment of Pathology, University of California, San Francisco, CA, USA.
Maria GuidoDepartment of Medicine-DIMED, Pathology Unit, University of Padova, Padova, Italy.
Bilal HameedDivision of Gastroenterology and Hepatology, Department of Medicine, University of California, San Francisco, San Francisco, California, USA.
Kenichi HaradaDepartment of Human Pathology, Kanazawa University Graduate School of Medicine, Kanazawa, Japan.
Prodromos HytiroglouDepartment of Pathology, Aristotle University Medical School, Thessaloniki, Greece.
Yasuni NakanumaDivision of Pathology, Shizuoka Cancer Center, Shizuoka, Japan, Department of Diagnostic Pathology, Fukui Prefecture Saiseikai Hospital, Fukui, Japan.
Valérie ParadisAP-HP, Hôpital Beaujon, Department of Pathology and Université Paris-Cité, Inserm UMR 1149, Clichy, France.
Pierre-Emmanuel RautouAP-HP, Hôpital Beaujon, Department of Hepatology and Université Paris-Cité, Inserm UMR 1149, Clichy, France.
Neil D TheiseDepartment of Pathology, New York University School of Medicine, New York, NY, USA.
Swan ThungDepartment of Pathology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Wilson Ms TsuiDepartment of Pathology, Caritas Medical Centre, Hong Kong.
Dale SnoverDepartment of Pathology, Fairview Southdale Hospital, Edina, MN, USA.
Ashley StueckDepartment of Pathology, Dalhousie University, Halifax, Nova Scotia, Canada.
Arief SuriawinataDepartment of Pathology and Laboratory Medicine, Dartmouth Hitchcock Medical Center, Lebanon, NH, 03756, USA.
Dirk J van LeeuwenSection of Gastroenterology and Hepatology, Geisel School of Medicine at Dartmouth College, Hanover, NH 03755, USA.
Alberto QuagliaDepartment of Cellular Pathology, Royal Free London NHS Foundation Trust, London, UK. Electronic address: alberto.quaglia@nhs.net.
International Liver Pathology Study Group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The lines defining Hepatocellular Adenoma (HCA) and Focal Nodular Hyperplasia (FNH) can be blurred when they occur outside their prototypical clinico-pathological contexts. A terminology going beyond HCA and FNH with comments on possible malignant potential, the status of the background liver and/or underlying unusual clinical scenario is thereby justified. Indeed, both more sophisticated contrast-enhanced characterization and the identification of specific immunohistochemical and molecular markers for well-differentiated hepatocellular lesions have enabled a greater understanding of their presentation and biology. The traditional concepts of HCA and FNH occurring in livers that are "otherwise histologically normal or near normal" has given way to understanding that these lesions can also occur in livers affected by chronic liver conditions. When this is the case, morpho-molecular overlap exists between the two entities. Hence, it is now necessary to set a new approach for HCA and FNH, considering not only their intrinsic morphologic and molecular features, but also the background liver in which they are arising, and the clinical context in which they are occurring. The dichotomous paradigm of benign vs. malignant also becomes more nuanced. To raise the diagnostic uncertainty in unusual clinico-pathological scenarios, the International Liver Pathology Study Group suggests designating these lesions as well-differentiated hepatocellular lesions, HCA-like (and subtype when applicable) or FNH-like. This nuanced terminology enables pathologists to highlight these outliers to the hepatobiliary multidisciplinary team that will adapt the clinical management accordingly. It also provides a framework for further collaborative studies. In conclusion, we propose a more nuanced terminology, beyond conventional HCA and FNH, to consider, alongside histological and molecular features, abnormalities in the background liver and unusual clinical scenarios.

Indexed as

alcohol-associated liver diseasebenignchronic liver diseaseclassificationfocal nodular hyperplasiaHepatocellular adenomamalignantmetabolic-associated steatotic liver diseasevascular liver disorders

Identifiers

PMID42034893
PMCPMC13127337

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.