Evidence map›Paper›PMID 41992682›Full record

ArticlePathology international2026

Eosinophilic Biliary Cystic Neoplasm of the Liver: A Case Report of an Unrecognized Subtype of Intrahepatic Biliary Neoplasm.

Mariko Tanaka, Daizo Koinuma, Munetoshi Hinata, Kimiko Takeshita, Yoichi Yasunaga, Kei Sakuma, Takeshi Takamoto, Yujiro Nishioka, Kiyoshi Hasegawa, Yudai Nakai and 1 more

Abstract readCase Reports
In one paragraph

Article in Pathology international, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Mariko TanakaDepartment of Pathology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.ORCID https://orcid.org/0000-0002-6877-9212
Daizo KoinumaDepartment of Pathology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Munetoshi HinataDepartment of Pathology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Kimiko TakeshitaDepartment of Pathology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Yoichi YasunagaDepartment of Pathology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.ORCID https://orcid.org/0000-0003-4809-7561
Kei SakumaDepartment of Pathology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Takeshi TakamotoDepartment of Hepatobiliary Pancreatic Surgery, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Yujiro NishiokaDepartment of Hepatobiliary Pancreatic Surgery, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Kiyoshi HasegawaDepartment of Hepatobiliary Pancreatic Surgery, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.ORCID https://orcid.org/0000-0001-8734-740X
Yudai NakaiDepartment of Radiology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Tetsuo UshikuDepartment of Pathology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.ORCID https://orcid.org/0000-0002-1763-8380

Funding

JSPS KAKENHI JP25K10245
6 · The paper itself

Abstract

We report a multicystic intrahepatic neoplasm in a 54-year-old Japanese woman, representing a previously unrecognized subtype. Grossly, the lesion was a well-demarcated multicystic tumor with focal papillary projections. Histologically, the cysts were lined by columnar to cuboidal neoplastic cells with brush border-like luminal microvilli, abundant granular eosinophilic cytoplasm, and small round nuclei. The cystic lumina contained colloid-like secretion, and bile-filled glands were occasionally observed. The septa were composed of thin hepatocellular parenchyma. Immunohistochemically, the tumor cells were positive for CD10, CK7, CK19, EpCAM, and SPINK1 and negative for HepPar1, MUC1, MUC2, MUC5AC, and MUC6. Whole-exome sequencing identified a pathogenic somatic KRAS p.G12V variant. RNA sequencing detected no PRKACA/B fusions. Single-cell spatial transcriptomics demonstrated that tumor cells clustered most closely with septal and medium-sized interlobular bile ducts. Gene set activity analysis showed significant suppression of gene sets downregulated by KRAS activation and upregulation of KRAS dependency signature gene sets in tumor cells. These findings distinguish this lesion from established entities of intrahepatic biliary cystic neoplasms, including intraductal papillary neoplasm, intraductal tubulopapillary neoplasm, intraductal oncocytic papillary neoplasm, and mucinous cystic neoplasm. We propose the designation "eosinophilic biliary cystic neoplasm of the liver" for this distinct intrahepatic biliary neoplasm.

Indexed as

Bile Duct NeoplasmsBile Ducts, IntrahepaticLiver NeoplasmsBiomarkers, TumorEosinophiliaFemaleHumansImmunohistochemistryMiddle AgedProto-Oncogene Proteins p21(ras)Biomarkers, TumorKRAS protein, humanProto-Oncogene Proteins p21(ras)eosinophilic cystic neoplasminterlobular bile ductintrahepatic biliary neoplasmKRAS pathogenic variant

Identifiers

PMID41992682
PMCPMC13087491

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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.