Evidence map›Paper›PMID 32845354›Full record

ArticleVirchows Archiv : an international journal of pathology2021

Renal cell carcinoma with leiomyomatous stroma in tuberous sclerosis complex: a distinct entity.

Marjorie Gournay, Frédéric Dugay, Marc-Antoine Belaud-Rotureau, Benoit Peyronnet, Romain Mathieu, Gregory Verhoest, Karim Bensalah, Sylvie Odent, Philippe Denizeau, Cécile Vigneau and 3 more

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In one paragraph

Article in Virchows Archiv : an international journal of pathology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

4 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Mutated ASXL1 upregulates mTOR expression in renal cell carcinoma with fibromyomatous stroma.Virchows Archiv : an international journal of pathology · 2024
    Article
  3. Review
  4. 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

13 authors at 4 institutions in 2 countries.

Marjorie GournayDepartment of Pathology, University Hospital, 2 rue Henri le Guilloux, 35000, Rennes, France. marjorie.gournay@chu-rennes.fr.ORCID http://orcid.org/0000-0003-3861-3067
Frédéric DugayDepartment of Cytogenetics, University Hospital, 35000, Rennes, France.
Marc-Antoine Belaud-RotureauDepartment of Cytogenetics, University Hospital, 35000, Rennes, France.
Benoit PeyronnetDepartment of Urology, University Hospital, 35000, Rennes, France.
Romain MathieuDepartment of Urology, University Hospital, 35000, Rennes, France.
Gregory VerhoestDepartment of Urology, University Hospital, 35000, Rennes, France.
Karim BensalahDepartment of Urology, University Hospital, 35000, Rennes, France.
Sylvie OdentDepartment of Genetic, University Hospital, 35000, Rennes, France.
Philippe DenizeauDepartment of Genetic, University Hospital, 35000, Rennes, France.
Cécile VigneauDepartment of Nephrology, University Hospital, 35000, Rennes, France.
Aurélien MoriniDepartment of Pathology, Georges Pompidou European Hospital, Paris, France.
Nathalie Rioux-LeclercqDepartment of Pathology, University Hospital, 2 rue Henri le Guilloux, 35000, Rennes, France.
Solène-Florence Kammerer-JacquetDepartment of Pathology, University Hospital, 2 rue Henri le Guilloux, 35000, Rennes, France.
Université Rennes 2 · FRCentre Hospitalier Universitaire de Rennes · FRInstitut de génétique et de développement de Rennes · FRAssistance Publique – Hôpitaux de Paris · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Renal cell carcinoma with leiomyomatous stroma (RCCLS) is an emerging entity frequently associated with tuberous sclerosis complex (TSC). We described herein a series of RCCLS in TSC patients at pathological and cytogenetic levels. Three male patients with TSC and RCCLS were identified between 2000 and 2019 at the University Hospital of Rennes. Histologically, the architecture was tubulo-papillary with thick bundles of smooth muscle cells. The tumor cells showed clear cytoplasm with eosinophilic globules. The immunohistochemical profile was identical with an intense positivity of CK7, CAIX, and CD10 and a heterogeneous positivity of CK20. SDHB was low but positive and TFE3 was not expressed. Comparative genomic hybridization (CGH) did not show any quantitative chromosome abnormality. No recurrence was observed with a median follow-up of 4 years. RCCLS in TSC patients has morphological, immunohistochemical, and cytogenetic distinct features that could constitute a distinct entity and a sentinel manifestation for the diagnosis of TSC.

Indexed as

AdultBiomarkers, TumorCarcinoma, Renal CellComparative Genomic HybridizationHumansImmunohistochemistryIn Situ Hybridization, FluorescenceKidney NeoplasmsLeiomyomaMaleTuberous SclerosisBiomarkers, TumorLeiomyomatous stromaRenal cell carcinomaTSC1TSC2Tuberous sclerosis complex

Identifiers

PMID32845354
OpenAlexW3080783307

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.