Evidence map›Paper›PMID 26516697›Full record

ArticleModern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc2016

Inflammatory hepatocellular adenomas developed in the setting of chronic liver disease and cirrhosis.

Julien Calderaro, Jean C Nault, Charles Balabaud, Gabrielle Couchy, Marie-Christine Saint-Paul, Daniel Azoulay, Dalila Mehdaoui, Alain Luciani, Elie S Zafrani, Paulette Bioulac-Sage and 1 more

Abstract read
PubMed Publisher
In one paragraph

Article in Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.7field-weighted citation impact, top 9% of its field
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

20 citing papers in PubMed, 54 citations in OpenAlex.

  1. Article
  2. Review
  3. Nonoperative Management of Hepatic Adenomas: A Review.Journal of gastrointestinal cancer · 2026
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Hepatocellular adenoma: Where are we now?World journal of gastroenterology · 2022
    Article
  12. Article
  13. Article
  14. Article
  15. Hepatocellular adenoma in men: A nationwide assessment of pathology and correlation with clinical course.Liver international : official journal of the International Association for the Study of the Liver · 2021
    Article
  16. Review
  17. Review
  18. Hepatocellular nodules in vascular liver diseases.Virchows Archiv : an international journal of pathology · 2018
    Review
  19. CT-MRI LI-RADS v2017: A Comprehensive Guide for Beginners.Journal of clinical and translational hepatology · 2018
    Review
  20. 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

11 authors at 4 institutions in 1 country.

Julien CalderaroDépartement de Pathologie, Assistance Publique-Hôpitaux de Paris, Centre Hospitalier Universitaire Henri Mondor, Créteil, France.
Jean C NaultInserm, UMR-1162, Génomique fonctionnelle des Tumeurs solides, Equipe Labellisée Ligue Contre le Cancer, Paris, France.
Charles BalabaudInserm, UMR-1053, Université Bordeaux Segalen, Bordeaux, France.
Gabrielle CouchyInserm, UMR-1162, Génomique fonctionnelle des Tumeurs solides, Equipe Labellisée Ligue Contre le Cancer, Paris, France.
Marie-Christine Saint-PaulDepartment of Pathology, CHU Pasteur, Nice, France.
Daniel AzoulayDepartment of Digestive and Hepatobiliary Surgery, Assistance Publique-Hôpitaux de Paris, Centre Hospitalier Universitaire Henri Mondor, Créteil, France.
Dalila MehdaouiDépartement de Pathologie, Assistance Publique-Hôpitaux de Paris, Centre Hospitalier Universitaire Henri Mondor, Créteil, France.
Alain LucianiDepartment of Medical Imaging, Assistance Publique-Hôpitaux de Paris, Centre Hospitalier Universitaire Henri Mondor, Créteil, France.
Elie S ZafraniDépartement de Pathologie, Assistance Publique-Hôpitaux de Paris, Centre Hospitalier Universitaire Henri Mondor, Créteil, France.
Paulette Bioulac-SageInserm, UMR-1053, Université Bordeaux Segalen, Bordeaux, France.
Jessica Zucman-RossiInserm, UMR-1162, Génomique fonctionnelle des Tumeurs solides, Equipe Labellisée Ligue Contre le Cancer, Paris, France.ORCID http://orcid.org/0000-0002-5687-0334
Centre Hospitalier Universitaire Henri-Mondor · FRDélégation Paris 5 · FRInserm · FRHôpital Pasteur · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatocellular adenoma is considered to occur exclusively in non-fibrotic livers. It is a heterogeneous entity and a molecular classification is now widely accepted. The most frequent hepatocellular adenoma subtype, namely inflammatory adenoma, harbor somatic activating mutations of genes involved in the interleukin-6 pathway that lead to high C-reactive protein and serum amyloid A expression. The aim of our study was to investigate a series of benign hepatocellular neoplasms developed on cirrhotic livers and characterized by an unequivocal histological diagnosis. We performed a clinical, pathological, and molecular study of 10 benign hepatocellular neoplasms developed in three patients with cirrhosis. Markers allowing hepatocellular adenoma classification were assessed by quantitative real-time PCR and immunohistochemistry. Samples were sequenced for CTNNB1, HNF1A, IL6ST, GNAS, STAT3, and TERT (promoter) mutations. A control series of 32 classical macronodules developed in cirrhosis related to various etiologies was screened by immunohistochemistry and gene sequencing. The three patients had cirrhosis related to metabolic syndrome and/or alcohol intake; two had a single tumor, while the third developed more than 30 lesions. Microscopic examination showed well-differentiated neoplasms sharing features with inflammatory adenoma including inflammatory infiltrates, sinusoidal dilatation, and dystrophic vessels. Sequencing revealed classical hotspot somatic mutations (IL6ST, n=8; STAT3, n=1; and GNAS, n=1) known to be responsible for IL-6/JAK/STAT pathway activation. Two classical high-grade macronodules demonstrated high serum amyloid A and/or C-reactive protein expression, without gene mutations. Altogether, our findings support the existence of rare inflammatory adenoma developed in cirrhosis.

Indexed as

Adenoma, Liver CellAdultbeta CateninChromograninsCytokine Receptor gp130End Stage Liver DiseaseFemaleGTP-Binding Protein alpha Subunits, GsHepatocyte Nuclear Factor 1-alphaHumansLiverLiver CirrhosisLiver NeoplasmsMaleMiddle AgedMutationbeta CateninChromograninsCTNNB1 protein, humanCytokine Receptor gp130GNAS protein, humanGTP-Binding Protein alpha Subunits, GsHepatocyte Nuclear Factor 1-alphaHNF1A protein, humanIL6ST protein, humanSTAT3 Transcription FactorTelomeraseTERT protein, human

Identifiers

PMID26516697
OpenAlexW2221301003

What OpenQuestion holds

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Registered trials

None linked

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.