Evidence map›Paper›PMID 40584698›Full record

ArticlePathology oncology research : POR2025

Low-grade oncocytic tumor of the kidney-a clinical, pathological, and next generation sequencing-based study of 20 tumors.

Alex Jenei, Boglárka Pósfai, Borbála Dénes, Áron Somorácz, Gertrud Forika, Attila Fintha, Zsófia Mészáros, Noémi Kránitz, Tamás Micsik, Kornélia Veronika Eizler and 16 more

Abstract read
In one paragraph

Article in Pathology oncology research : POR, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. 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

26 authors.

Alex JeneiDepartment of Pathology and Experimental Cancer Research, Faculty of Medicine, Semmelweis University, Budapest, Hungary.
Boglárka PósfaiDepartment of Pathology, Albert Szent-Györgyi Medical School, University of Szeged, Szeged, Hungary.
Borbála DénesEurofins-MedServ Ltd., Budapest, Hungary.
Áron SomoráczEurofins-MedServ Ltd., Budapest, Hungary.
Gertrud ForikaDepartment of Pathology and Experimental Cancer Research, Faculty of Medicine, Semmelweis University, Budapest, Hungary.
Attila FinthaDepartment of Pathology and Experimental Cancer Research, Faculty of Medicine, Semmelweis University, Budapest, Hungary.
Zsófia MészárosPathology Unit, Győr-Moson-Sopron Shire Aladár Petz University Teaching Hospital, Győr, Hungary.
Noémi KránitzPathology Unit, Győr-Moson-Sopron Shire Aladár Petz University Teaching Hospital, Győr, Hungary.
Tamás MicsikDepartment of Pathology and Experimental Cancer Research, Faculty of Medicine, Semmelweis University, Budapest, Hungary.
Kornélia Veronika EizlerPathology Unit, Fejér Shire Saint George University Teaching Hospital, Székesfehérvár, Hungary.
Nándor GibaPathology Unit, Fejér Shire Saint George University Teaching Hospital, Székesfehérvár, Hungary.
Dávid SemjénDepartment of Pathology, Medical School and Clinical Centre, University of Pécs, Pécs, Hungary.
Dóra KelemenPathology Unit, Uzsoki Street Hospital, Budapest, Hungary.
Ferenc SalamonPathology Unit, Uzsoki Street Hospital, Budapest, Hungary.
Anna SchubertDepartment of Pathology, Albert Szent-Györgyi Medical School, University of Szeged, Szeged, Hungary.
Gábor CserniDepartment of Pathology, Albert Szent-Györgyi Medical School, University of Szeged, Szeged, Hungary.
Adrienn HajduMedipredict Ltd., Budapest, Hungary.
Luca VargaDepartment of Pathology and Experimental Cancer Research, Faculty of Medicine, Semmelweis University, Budapest, Hungary.
Balázs ÁrvaiDepartment of Pathology and Experimental Cancer Research, Faculty of Medicine, Semmelweis University, Budapest, Hungary.
Dániel SztankovicsDepartment of Pathology and Experimental Cancer Research, Faculty of Medicine, Semmelweis University, Budapest, Hungary.
Anna SebestyénDepartment of Pathology and Experimental Cancer Research, Faculty of Medicine, Semmelweis University, Budapest, Hungary.
Fanni SántaDepartment of Radiology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, United States.
Andrea SimonDepartment of Surgical and Molecular Pathology, Tumor Pathology Center, National Institute of Oncology, Budapest, Hungary.
Helga EngiDepartment of Surgical and Molecular Pathology, Tumor Pathology Center, National Institute of Oncology, Budapest, Hungary.
Zsombor MeleghDepartment of Surgical and Molecular Pathology, Tumor Pathology Center, National Institute of Oncology, Budapest, Hungary.
Levente KuthiDepartment of Pathology and Experimental Cancer Research, Faculty of Medicine, Semmelweis University, Budapest, Hungary.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Low-grade oncocytic tumor (LOT) of the kidney is a recently recognized renal neoplasm with distinctive morphologic, immunophenotypic, and molecular features that distinguish it from other eosinophilic tumors such as oncocytoma and chromophobe renal cell carcinoma (chRCC). This study presents a comprehensive analysis of 20 LOTs from 19 patients, integrating clinicopathological, immunohistochemical, and genetic data. LOTs typically appeared as small, unilateral, well-circumscribed tumors with a tan-brown cut surface, composed of uniform eosinophilic cells with round nuclei and occasional perinuclear halos. Key histological hallmarks included an extensive capillary network and central edematous areas without necrosis or significant atypia. Immunohistochemically, all tumors showed strong diffuse CK7 positivity and CD117 negativity, with universal expression of GATA3, GPNMB, and L1CAM. Whole-exome and panel-based sequencing revealed recurrent mutations in the mTOR signaling pathway, including

Indexed as

Adenoma, OxyphilicBiomarkers, TumorCarcinoma, Renal CellKidney NeoplasmsAdultAgedFemaleFollow-Up StudiesHigh-Throughput Nucleotide SequencingHumansMaleMiddle AgedMutationPrognosisBiomarkers, Tumorkidney tumorLOTmTOR pathwayNGSWES

Identifiers

PMID40584698
PMCPMC12203018

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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.