Evidence map›Paper›PMID 41073540›Full record

ArticleVirchows Archiv : an international journal of pathology2025

Uterine mesenchymal tumour with a novel EWSR1::CTBP1 gene fusion.

Beata Bode-Lesniewska, Frank Illigen, Matthias S Matter

Abstract readCase Reports
In one paragraph

Article in Virchows Archiv : an international journal of pathology, 2025. 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

3 authors.

Beata Bode-LesniewskaInstitute of Pathology, Cantonal Hospital Lucerne, Lucerne and University of Zurich, CH-6000, Lucerne, Switzerland. beata.bode@luks.ch.ORCID https://orcid.org/0000-0002-3329-4186
Frank IlligenGynecology, Zug, Switzerland.
Matthias S MatterInstitute of Medical Genetics and Pathology, University Hospital of Basel, Basel, Switzerland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A growing number of mesenchymal uterine tumours are defined by a specific molecular aberration. We present the case of a 65-year-old woman who presented with postmenopausal bleeding and a large intramural uterine tumour. Histopathological analysis of the resected uterus revealed an intramural, mesenchymal neoplasm comprising of spindle and epithelioid cells, with no immunohistochemical expression of lineage-specific markers and low proliferative activity. Molecular testing using next-generation sequencing (NGS) revealed an EWSR1::CTBP1 gene fusion, which was confirmed by the presence of EWSR1 gene rearrangement detected using fluorescence in situ hybridisation (FISH). Staging revealed no further tumour manifestations, and the 3-year follow-up was uneventful. The EWSR1::CTBP1 gene fusion has never previously been reported in uterine tumours, having been reported in the literature only once, in the context of a gastroblastoma. The presented case expands the range of the gene-fusion-associated mesenchymal tumours of the uterus.

Indexed as

Biomarkers, TumorDNA-Binding ProteinsGene FusionMesenchymomaRNA-Binding Protein EWSUterine NeoplasmsAgedFemaleHumansIn Situ Hybridization, FluorescenceBiomarkers, TumorDNA-Binding ProteinsEWSR1 protein, humanRNA-Binding Protein EWSFISHMesenchymal tumoursNext-generation sequencingUterus

Identifiers

PMID41073540
PMCPMC12647275

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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.