Evidence map›Paper›PMID 37695410›Full record

ArticleVirchows Archiv : an international journal of pathology2023

Androgenetic/biparental mosaicism in a diploid mole-like conceptus: report of a case with triple paternal contribution.

Marie Donzel, Lucie Gaillot-Durand, Madeleine Joubert, Jacqueline Aziza, Claire Beneteau, Claire Mauduit, Stéphane Ploteau, Touria Hajri, Pierre-Adrien Bolze, Jérôme Massardier and 3 more

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In one paragraph

Article in Virchows Archiv : an international journal of pathology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 7 institutions in 2 countries.

Marie DonzelDepartment of Pathology, Hospices Civils de Lyon, Centre Hospitalier Lyon Sud, 165 Chemin du Grand Revoyet, 69495, Pierre-Benite Cedex, France.
Lucie Gaillot-DurandDepartment of Pathology, Hospices Civils de Lyon, Centre Hospitalier Lyon Sud, 165 Chemin du Grand Revoyet, 69495, Pierre-Benite Cedex, France.
Madeleine JoubertDepartment of Pathology, University Hospital Hôtel Dieu, Nantes, France.
Jacqueline AzizaFrench Reference Center for Gestational Trophoblastic Diseases, Hospices Civils de Lyon, Centre Hospitalier Lyon Sud, Pierre-Benite, France.
Claire BeneteauDepartment of Human Genetics, University Hospital Hôtel Dieu, Nantes, France.
Claire MauduitDepartment of Pathology, Hospices Civils de Lyon, Centre Hospitalier Lyon Sud, 165 Chemin du Grand Revoyet, 69495, Pierre-Benite Cedex, France.
Stéphane PloteauDepartment of Gynecology and Obstetrics, University Hospital Hôtel Dieu, Nantes, France.
Touria HajriFrench Reference Center for Gestational Trophoblastic Diseases, Hospices Civils de Lyon, Centre Hospitalier Lyon Sud, Pierre-Benite, France.
Pierre-Adrien BolzeFrench Reference Center for Gestational Trophoblastic Diseases, Hospices Civils de Lyon, Centre Hospitalier Lyon Sud, Pierre-Benite, France.
Jérôme MassardierFrench Reference Center for Gestational Trophoblastic Diseases, Hospices Civils de Lyon, Centre Hospitalier Lyon Sud, Pierre-Benite, France.
Mojgan Devouassoux-ShisheboranDepartment of Pathology, Hospices Civils de Lyon, Centre Hospitalier Lyon Sud, 165 Chemin du Grand Revoyet, 69495, Pierre-Benite Cedex, France.
Lone SundeDepartment of Human Genetics, University Hospital, Aalborg, Denmark.
Fabienne AlliasDepartment of Pathology, Hospices Civils de Lyon, Centre Hospitalier Lyon Sud, 165 Chemin du Grand Revoyet, 69495, Pierre-Benite Cedex, France. fabienne.allias@chu-lyon.fr.ORCID http://orcid.org/0000-0002-6663-1492
Hospices Civils de Lyon · FRCentre Hospitalier Universitaire de Nantes · FRUniversité Claude Bernard Lyon 1 · FRAalborg University Hospital · DKCentre Hospitalier Universitaire de Tours · FRHôpital Femme Mère Enfant · FRInstitut universitaire du cancer de Toulouse Oncopole · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hydatidiform moles (HMs) are divided into two types: partial hydatidiform mole (PHM) which is most often diandric monogynic triploid and complete hydatidiform mole (CHM) which is most often diploid androgenetic. Morphological features and p57 immunostaining are routinely used to distinguish both entities. Genetic analyses are required in challenging cases to determine the parental origin of the genome and ploidy. Some gestations cannot be accurately classified however. We report a case with atypical pathologic and genetic findings that correspond neither to CHM nor to PHM. Two populations of villi with divergent and discordant p57 expression were observed: morphologically normal p57 + villi and molar-like p57 discordant villi with p57 + stromal cells and p57 - cytotrophoblasts. Genotyping of DNA extracted from microdissected villi demonstrated that the conceptus was an androgenetic/biparental mosaic, originating from a zygote with triple paternal contribution, and that only the p57 - cytotrophoblasts were purely androgenetic, increasing the risk of neoplastic transformation.

Indexed as

Hydatidiform MoleUterine NeoplasmsCyclin-Dependent Kinase Inhibitor p57DiploidyFemaleGenotypeHumansImmunohistochemistryMosaicismPregnancyCyclin-Dependent Kinase Inhibitor p57AndrogeneticGestational trophoblastic diseaseHydatidiform moleInverted discordant p57 expressionMolecular genotypingMosaicism

Identifiers

PMID37695410
OpenAlexW4386592878

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.