Evidence map›Paper›PMID 41036703›Full record

ArticleThe American journal of surgical pathology2026

PRRX1 -rearranged Fibroblastic Tumors : A Clinicopathologic and Molecular Study of 18 Cases Including a Novel PRRX1::EP300 Fusion.

Carina A Dehner, Jorge Torres-Mora, Judith Jebastin Thangaiah, Andre Oliveira, Michael Michal, Faizan Malik, Nasir Ud Din, Usman Hassan, Hina Maqbool, Farres Obeidin and 13 more

Abstract read
In one paragraph

Article in The American journal of surgical pathology, 2026. 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
–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

2 citing papers in PubMed.

  1. Article
  2. International journal of surgical pathology · 2026
    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

23 authors.

Carina A DehnerDepartment of Pathology, Indiana University School of Medicine, Indianapolis, IN.
Jorge Torres-MoraDepartment of Pathology and Immunology, Mayo Clinic, Rochester, MN.
Judith Jebastin ThangaiahDepartment of Pathology and Immunology, Mayo Clinic, Rochester, MN.
Andre OliveiraDepartment of Pathology and Immunology, Mayo Clinic, Rochester, MN.
Michael MichalDepartment of Pathology, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic.
Faizan MalikDepartment of Pathology, St. Jude Children's Research Hospital, Memphis, TN.
Nasir Ud DinUniversity of Miami Miller School of Medicine, Department of Pathology and Laboratory Medicine, Miami, FL.
Usman HassanDepartment of Histopathology, Shaukat Khanum Memorial Cancer Hospital and Research Center, Lahore, Pakistan.
Hina MaqboolDepartment of Histopathology, Shaukat Khanum Memorial Cancer Hospital and Research Center, Lahore, Pakistan.
Farres ObeidinDepartment of Pathology, Northwestern University Feinberg School of Medicine, Chicago, IL.
Mara CarageaDepartment of Laboratory Medicine and Pathology, University of Alberta, Edmonton, AB, Canada.
Cheng-Han LeeDepartment of Laboratory Medicine and Pathology, University of Alberta, Edmonton, AB, Canada.
Christian SchubartInstitute of Pathology, Friedrich-Alexander-University Erlangen-Nurnberg, University Hospital, Erlangen, Germany.
Abbas AgaimyInstitute of Pathology, Friedrich-Alexander-University Erlangen-Nurnberg, University Hospital, Erlangen, Germany.
Bo GrundtmannDepartment of Breast Surgery, Zealand University Hospital, Roskilde, Denmark.
Linea MelchiorDepartment of Pathology, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.
Maj-Lis TalmanDepartment of Pathology, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.
John GrossDepartment of Pathology, The Johns Hopkins Hospital, Baltimore, MD.
Alison L CheahDouglass Hanly Moir Pathology, 14 Giffnock Avenue, Macquarie Park, NSW, Australia.
Khin ThwayDivision of Molecular Pathology, The Institute of Cancer Research, London, United Kingdom.
Cyril FisherDivision of Molecular Pathology, The Institute of Cancer Research, London, United Kingdom.
Cristina R AntonescuDepartment of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
Konstantinos LinosDepartment of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0001-9462-652

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

With the first series of PRRX1 -rearranged tumors published in 2019, the spectrum of these so-called fibroblastic tumors has been expanded. Since then, several smaller case series have been published; however, our understanding of them continues to be quite limited given their rarity. We herein studied 18 additional cases, the largest series to date. Eighteen tumors present in 9 male, 8 female, and 1 nonbinary patient with a median age of 35 years (range: 11 to 70 y) and involved the neck (5), the chest region (4), thigh (3), back (1), shoulder (1), forehead (1), lower leg (1), axilla (1), and the parapharyngeal region (1). Clinical follow-up (9/18 tumors; 50%; median: 10 mo; range: 4 to 40 mo) showed consistent indolent behavior without local recurrences or distant metastases. On morphology, these tumors were characterized by well-circumscription and distinctive peripheral crescent-shaped vessels. They were composed of uniform spindle and round cells growing in short fascicles within often densely hyalinized collagen lacking significant mitotic activity, necrosis, or cytologic atypia. Immunohistochemically, about half of the tested tumors expressed focal to rarely diffuse S100 with occasional co-expression of SOX10. Interestingly, almost half of the tested cases also showed complete loss of RB expression. All but 1 tumor harbored a PRRX1::NCOA1 fusion, while 1 case harbored a novel PRRX1::EP300 fusion. We herein provide additional data on these exceptionally uncommon tumors, expand their molecular spectrum, and compare them to their close morphologic mimics to aid in accurate diagnosis and avoid confusion with potentially more aggressive neoplasms.

Indexed as

Biomarkers, TumorE1A-Associated p300 ProteinHomeodomain ProteinsSoft Tissue NeoplasmsAdolescentAdultAgedChildFemaleFollow-Up StudiesGene RearrangementHumansMaleMiddle AgedNuclear Receptor Coactivator 1Young AdultBiomarkers, TumorE1A-Associated p300 ProteinEP300 protein, humanHomeodomain ProteinsNCOA1 protein, humanNuclear Receptor Coactivator 1PRRX1 protein, humanfibroblastic tumor

Identifiers

PMID41036703
PMCPMC13439680

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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.