Evidence map›Paper›PMID 41078400›Full record

ArticleCase reports in pathology2025

Intracholecystic Papillary Neoplasm With Associated Invasive Carcinoma, Accompanied by Tumor Thrombi of Hepatoid Adenocarcinoma: A Case Report.

Sho Yoshida, Yusuke Kouchi, Ryotaro Eto, Masayuki Ohtsuka, Takashi Kishimoto

Abstract readCase Reports
In one paragraph

Article in Case reports in pathology, 2025. 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. Article
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

5 authors.

Sho YoshidaChiba University School of Medicine, Chiba, Japan.
Yusuke KouchiDepartment of Molecular Pathology, Chiba University Graduate School of Medicine, Chiba, Japan.ORCID https://orcid.org/0000-0002-3434-1263
Ryotaro EtoDepartment of General Surgery, Chiba University Graduate School of Medicine, Chiba, Japan.ORCID https://orcid.org/0000-0001-5245-3149
Masayuki OhtsukaDepartment of General Surgery, Chiba University Graduate School of Medicine, Chiba, Japan.ORCID https://orcid.org/0000-0002-5091-1078
Takashi KishimotoDepartment of Molecular Pathology, Chiba University Graduate School of Medicine, Chiba, Japan.ORCID https://orcid.org/0000-0002-7552-7259

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatoid adenocarcinoma (HAC) is a rare extrahepatic adenocarcinoma characterized by hepatocellular differentiation. HAC arising in the gallbladder is rare. We report a case of intracholecystic papillary neoplasm (ICPN) with HAC, most of which were tumor thrombi. The patient was a 78-year-old Japanese woman diagnosed with a gallbladder mass, detected by ultrasonography. She underwent cholecystectomy with lymph node dissection. Histopathological examination revealed exophytic papillary growth consistent with ICPN with associated invasive carcinoma. Notably, many tumor nests displayed characteristics of HAC, including eosinophilic granular cytoplasm and solid trabecular patterns. Immunohistochemically, tumor cells were positive for AFP, Glypican 3, and Hep Par 1 but negative for SALL4. Our findings underscore the importance of recognizing HAC components in gallbladder lesions, particularly in the context of ICPN with associated invasive carcinoma, as they may significantly impact patient prognosis.

Indexed as

gallbladderhepatoid adenocarcinomaintracholecystic papillary neoplasmSALL4tumor thrombi

Identifiers

PMID41078400
PMCPMC12513791

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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.