Evidence map›Paper›PMID 42500196›Full record

ArticleRevista brasileira de ginecologia e obstetricia : revista da Federacao Brasileira das Sociedades de Ginecologia e Obstetricia2026

Insights about use of p57 in differentiation between complete and partial hydatidiform mole: a scoping review.

Isabelle Sasso Teixeira, Sheldon Rodrigo Botogoski, Renato Nisihara

Abstract readScoping Review
In one paragraph

Article in Revista brasileira de ginecologia e obstetricia : revista da Federacao Brasileira das Sociedades de Ginecologia e Obstetricia, 2026. 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.

Isabelle Sasso TeixeiraUniversidade Federal do Paraná Paraná Brazil Universidade Federal do Paraná, Curitiba, Paraná, Brazil.ORCID https://orcid.org/0000-0003-2135-9314
Sheldon Rodrigo BotogoskiUniversidade Federal do Paraná Paraná Brazil Universidade Federal do Paraná, Curitiba, Paraná, Brazil.ORCID https://orcid.org/0000-0002-1676-7826
Renato NisiharaUniversidade Federal do Paraná Paraná Brazil Universidade Federal do Paraná, Curitiba, Paraná, Brazil.ORCID https://orcid.org/0000-0002-1234-8093

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: To assess the utility of p57 in differentiating histological subtypes of hydatidiform mole and its applicability in clinical practice. Methods: A scoping review was conducted following the Joanna Briggs Institute methodology and PRISMA-ScR guidelines. The article search was conducted in the PubMed, EMBASE, BVS, Cochrane, Web of Science, and Scopus databases. Studies published between 2015 and 2025 that evaluated the use of p57 in suspected cases of hydatidiform mole were included. Results: Nine studies met the inclusion criteria. Most demonstrated high specificity of p57 for CHM diagnosis and a significant reduction in diagnostic discordance compared to morphology alone. However, p57 does not distinguish PHM from non-molar abortions. In addition, rare cases of divergent p57 expression were reported, associated with genetic alterations that may require complementary evaluation using molecular techniques. Conclusion: IHC for p57 is a widely accessible, low-cost, and effective tool in clinical practice, particularly useful in resource-limited settings. Its routine use, in association with morphology and molecular methods when available, contributes to more accurate diagnoses and safer clinical management of GTDs.

Indexed as

Cyclin-Dependent Kinase Inhibitor p57Hydatidiform MoleUterine NeoplasmsDiagnosis, DifferentialFemaleHumansPregnancyCDKN1C protein, humanCyclin-Dependent Kinase Inhibitor p57Cyclin dependent kinase inhibitor P57Gestational trophoblastic diseaseHydatidiform moleImmunohistochemistryP57 protein

Identifiers

PMID42500196
PMCPMC13399369

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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.