Evidence map›Paper›PMID 42401947›Full record

ArticleActa neuropathologica communications2026

Challenging anatomical paradigms: unexpected supratentorial localization of posterior fossa B ependymomas identified by DNA methylation.

Pedro Piovesan Lago, Mariana Maschietto, Marllon Cindra Sant'Ana, Carlos Eduardo Ramos Fernandes, João Victor Alves de Castro, Felipe D'Almeida Costa, María Soledad Vega-Delgado, Julia Gabriela Ramos da Costa, Antonio Carlos Dos Santos, Ricardo Santos de Oliveira and 4 more

Abstract readCase Reports
In one paragraph

Article in Acta neuropathologica communications, 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

14 authors.

Pedro Piovesan Lago *Department of Pathology, A.C.Camargo Cancer Center, São Paulo, Brazil.ORCID http://orcid.org/0009-0004-9281-3566
Mariana Maschietto *Research Center, Boldrini Children's Center, Campinas, São Paulo, Brazil.ORCID http://orcid.org/0000-0003-2589-3186
Marllon Cindra Sant'AnaDepartment of Pediatrics, Ribeirão Preto Medical School, University of São Paulo, Av Bandeirantes 3900 - Bairro Monte Alegre - HC Criança, 5o andar - Departamento de Puericultura e Pediatria - sala 505, Ribeirao Preto, Brazil.ORCID http://orcid.org/0009-0002-5542-7020
Carlos Eduardo Ramos FernandesDepartment of Pediatric Oncology, A.C. Camargo Cancer Center, São Paulo, SP, 14048-900, Brazil.ORCID http://orcid.org/0000-0003-2610-269X
João Victor Alves de CastroDepartment of Pathology, A.C.Camargo Cancer Center, São Paulo, Brazil.ORCID http://orcid.org/0000-0002-1279-3672
Felipe D'Almeida CostaDepartment of Pathology, A.C.Camargo Cancer Center, São Paulo, Brazil.ORCID http://orcid.org/0000-0002-6470-749X
María Soledad Vega-DelgadoDepartment of Pediatrics, Ribeirão Preto Medical School, University of São Paulo, Av Bandeirantes 3900 - Bairro Monte Alegre - HC Criança, 5o andar - Departamento de Puericultura e Pediatria - sala 505, Ribeirao Preto, Brazil.ORCID http://orcid.org/0000-0003-2968-3303
Julia Gabriela Ramos da CostaDepartment of Pediatrics, Ribeirão Preto Medical School, University of São Paulo, Av Bandeirantes 3900 - Bairro Monte Alegre - HC Criança, 5o andar - Departamento de Puericultura e Pediatria - sala 505, Ribeirao Preto, Brazil.ORCID http://orcid.org/0009-0002-6097-1995
Antonio Carlos Dos SantosDepartment of Medical Imaging, Hematology and Oncology, Ribeirao Preto Medical School, University of São Paulo, Ribeirao Preto, SP, Brazil.ORCID http://orcid.org/0000-0002-5502-4734
Ricardo Santos de OliveiraDivision of Neurosurgery, Department of Surgery and Anatomy, Ribeirão Preto Medical School, University of São Paulo, Ribeirao Preto, SP, Brazil.ORCID http://orcid.org/0000-0003-0390-5553
Marcelo Volpon SantosDivision of Neurosurgery, Department of Surgery and Anatomy, Ribeirão Preto Medical School, University of São Paulo, Ribeirao Preto, SP, Brazil.ORCID http://orcid.org/0000-0002-0850-7039
Diego Souza Lima FonsecaDepartment of Medical Imaging, Hematology and Oncology, Ribeirao Preto Medical School, University of São Paulo, Ribeirao Preto, SP, Brazil.
Carlos Alberto ScrideliDepartment of Pediatrics, Ribeirão Preto Medical School, University of São Paulo, Av Bandeirantes 3900 - Bairro Monte Alegre - HC Criança, 5o andar - Departamento de Puericultura e Pediatria - sala 505, Ribeirao Preto, Brazil.ORCID http://orcid.org/0000-0001-6618-789X
Elvis Terci ValeraDepartment of Pediatrics, Ribeirão Preto Medical School, University of São Paulo, Av Bandeirantes 3900 - Bairro Monte Alegre - HC Criança, 5o andar - Departamento de Puericultura e Pediatria - sala 505, Ribeirao Preto, Brazil. etvalera@fmrp.usp.br.ORCID http://orcid.org/0000-0002-4434-429X

Funding

Brazilian Ministry of Health - MoH (Programa Nacional de Genômica e Saúde de Precisão - Genomas Brasil) and National Council for Scientific and Technological Development - CNPq 406716/2022-6
6 · The paper itself

Abstract

Molecular subgroups of ependymomas are strongly associated with their primary anatomical compartments, namely the supratentorial region, posterior fossa and spine locations. Although it is generally accepted that posterior fossa ependymomas may arise from radial glia-like progenitor cells, the precise cellular origin of the distinct posterior fossa molecular subgroups remains to be determined. Given that DNA methylation profile strongly recapitulates developmental lineage and the cell of origin, the characterization of unexpectedly located molecular subgroups of ependymomas may provide insights into their cells of origin and potential migratory dynamics during embryogenesis and brain development. Herein, we describe two male school-aged pediatric patients with supratentorial tumors located in the third ventricle/pineal region that were classified as posterior fossa group B ependymomas based on DNA methylation profiling. To our knowledge, this represents the first reports of posterior fossa group B ependymomas identified outside the posterior fossa compartment.

Indexed as

DNA MethylationEpendymomaInfratentorial NeoplasmsSupratentorial NeoplasmsChildHumansMagnetic Resonance ImagingMaleBrain neoplasmsChildhood ependymomaDiagnosisDifferentialDNA methylationNeurosurgical procedures

Identifiers

PMID42401947
PMCPMC13613717

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