Evidence map›Paper›PMID 41870614›Full record

ArticleVirchows Archiv : an international journal of pathology2026

The acinar variant of poroma: a series of 3 cases with YAP1::NR4A3 fusion.

Jeanne Breton, Daniel Pissaloux, Kerman Zyani, Sebastien Taix, Christelle Zardi, Nicolas Ortonne, Thibault Kervarrec

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Article in Virchows Archiv : an international journal of pathology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Jeanne BretonDepartment of Pathology, Université de Tours, Centre Hospitalier Universitaire de Tours, Tours, France.
Daniel PissalouxDepartment of Biopathology, Centre Léon Bérard, Lyon, France.
Kerman ZyaniDepartment of Pathology, Université de Tours, Centre Hospitalier Universitaire de Tours, Tours, France.
Sebastien TaixDepartment of Pathology, MEDIPATH, Marseille, France.
Christelle ZardiDepartment of Pathology, Assistance Publique - Hopitaux de Paris (AP-HP), Henri Mondor Hospital, Créteil, France.
Nicolas OrtonneDepartment of Pathology, Assistance Publique - Hopitaux de Paris (AP-HP), Henri Mondor Hospital, Créteil, France.
Thibault KervarrecDepartment of Pathology, Université de Tours, Centre Hospitalier Universitaire de Tours, Tours, France. thibaultkervarrec@yahoo.fr.ORCID http://orcid.org/0000-0002-2201-6914

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Poromas are benign sweat gland adnexal neoplasms that include four distinct architectural variants i.e. classical poroma, hidroacanthoma simplex, poroid hidradenoma and dermal duct tumor. Most of the poromas display oncogenic YAP1::MAML2 or YAP1::NUTM1 fusions and previous studies have suggested a correlation between the YAP1's fusion partner and the tumor morphology. Recently, two cases of YAP1::NR4A3 fused-poromas with distinctive morphology have been described. Herein we described 3 additional cases of YAP1::NR4A3 fused-poromas. All specimens harbored a biphasic appearance with a superficial part composed of anastomosing strands of monotonous poroid cells, while the deepest portion was organized as micronodules containing numerous glandular formations with eosinophilic secretory material. Immunohistochemistry revealed loss of YAP1 expression in both tumor parts. Targeted RNA sequencing confirmed the presence of an in frame YAP1::NR4A3 fusion transcript in two cases. NR4A3 rearrangement was demonstrated by FISH in the last specimen. To conclude, we report three cases of poromas with YAP1::NR4A3 fusions, confirming these tumors as a distinctive morphologic variant of poroma and proposed the term "acinar variant" for this latter.

Indexed as

Adaptor Proteins, Signal TransducingBiomarkers, TumorDNA-Binding ProteinsPoromaReceptors, SteroidReceptors, Thyroid HormoneSweat Gland NeoplasmsTranscription FactorsGene FusionHumansImmunohistochemistryOncogene Proteins, FusionYAP-Signaling ProteinsAdaptor Proteins, Signal TransducingBiomarkers, TumorDNA-Binding ProteinsNR4A3 protein, humanOncogene Proteins, FusionReceptors, SteroidReceptors, Thyroid HormoneTranscription FactorsYAP1 protein, humanYAP-Signaling ProteinsGene fusionNR4A3Poroid adnexal tumorPoromaYAP1

Identifiers

PMID41870614

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