Evidence map›Paper›PMID 27830327›Full record

ArticleVirchows Archiv : an international journal of pathology2017

Lack of mutation of DICER1 and FOXL2 genes in microcystic stromal tumor of the ovary.

Alexandra Meurgey, Françoise Descotes, Eliane Mery-Lamarche, Mojgan Devouassoux-Shisheboran

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In one paragraph

Article in Virchows Archiv : an international journal of pathology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Review
  2. Ovarian microcystic stromal tumor: a case report and literature review.International journal of clinical and experimental pathology · 2025
    Article
  3. Review
  4. Review
  5. Article
  6. Ovarian microcystic stromal tumors: clinical, radiological, and pathological studies of two cases.International journal of clinical and experimental pathology · 2019
    Article
  7. 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

4 authors.

Alexandra MeurgeyDepartment of Pathology, Hospices Civils de Lyon, Centre Hospitalier Lyon Sud, Université Lyon I, 165 Chemin du Grand Revoyet, 69310, Pierre-Bénite, France.
Françoise DescotesDepartment of Molecular Biology, Hospices Civils de Lyon, Centre hospitalier Lyon Sud, 165 Chemin du Grand Revoyet, 69310, Pierre-Bénite, France.
Eliane Mery-LamarcheDepartement of Pathology, Institut Universitaire du Cancer Toulouse, Oncopole 1 Avenue Irène Jolliot-Curie Cedex 9, 31059, Toulouse, France.
Mojgan Devouassoux-ShisheboranDepartment of Pathology, Hospices Civils de Lyon, Centre Hospitalier Lyon Sud, Université Lyon I, 165 Chemin du Grand Revoyet, 69310, Pierre-Bénite, France. mojgan.devouassoux@chu-lyon.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Microcystic stromal tumors (MCST), first described in 2009 by Irving et al., are rare ovarian neoplasms. The entity was introduced into the 2014 WHO classification of tumors of female reproductive organs in the group of sex cord-stromal tumors, which is rather heterogeneous. We studied three cases of ovarian tumor with the characteristic morphological features and immunohistochemical marker profiles of MCST. The three tumors showed micro, and macrocystic patterns with solid areas, and were composed of small round to spindle-shaped cells, without atypia. The tumors diffusely and strongly expressed CD10, FOXL2, and nuclear β-catenin, but without immmunoreactivity for hormone receptors, calretinin, or inhibin. Genome analyses showed no somatic mutation of exon 1 of the FOXL2 gene and of exons 24 and 25 of DICER1 gene, the latter not having been reported previously. The patients are well, without evidence of tumor progression 1 to 10 years after diagnosis.The absence of FOXL2 and DICER1 gene mutation, along with strong FOXL2 immunoreactivity provides additional evidence to place MCST within pure gonadal stromal rather than sex cord ovarian tumors.

Indexed as

MutationBiomarkers, TumorDEAD-box RNA HelicasesFemaleForkhead Box Protein L2Forkhead Transcription FactorsHumansMiddle AgedOvarian NeoplasmsRibonuclease IIISex Cord-Gonadal Stromal TumorsBiomarkers, TumorDEAD-box RNA HelicasesDICER1 protein, humanForkhead Box Protein L2Forkhead Transcription FactorsFOXL2 protein, humanRibonuclease IIIDICER1FOXL2Microcystic stromal tumorOvarySex-cord stromal tumors

Identifiers

What OpenQuestion holds

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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.