Evidence map›Paper›PMID 41960922›Full record

ArticleJournal of pediatric hematology/oncology2026

Intraosseous Venous Malformation of the Rib With EWSR1-NFATC1 Fusion Mimicking Malignancy: A Pediatric Case Report.

Bridgette McCarty, Heather Gochnauer, Xochitl Longstaff, Angelina Labib, John Naheedy, Art Kulatti, Jun Q Mo, Natalie Ellington, Hilda Ding, Karen Lee and 3 more

Abstract readCase Reports
In one paragraph

Article in Journal of pediatric hematology/oncology, 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

13 authors.

Bridgette McCartyUniversity of California.
Heather GochnauerDivisions of Dermatology.
Xochitl LongstaffDivisions of Dermatology.
Angelina LabibDivisions of Dermatology.
John NaheedyRadiology.
Art KulattiUniversity of California.
Jun Q MoUniversity of California.
Natalie EllingtonUniversity of California.
Hilda DingUniversity of California.
Karen LeeUniversity of California.
Benjamin KellerUniversity of California.
Dawn EichenfieldDivisions of Dermatology.
Deborah SchiffUniversity of California.ORCID 0000-0003-3154-8987

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIntraosseous venous malformations are rare, benign vascular bone lesions that may mimic malignant sarcomas on imaging. OBSERVATIONS: A 14-year-old male presented with fever and cough. Imaging revealed an incidental ossified rib mass with aggressive features. CT-guided biopsy was nondiagnostic, whereas open biopsy demonstrated a vascular lesion positive for CD31, FLI-1, and ERG. Molecular testing identified an EWSR1-NFATC1 fusion. Gross total resection was achieved, followed by prolonged disease-free survival, and the patient resumed full athletic activity 7 months after surgery.

conclusionsThis case highlights the value of open biopsy and molecular testing to prevent misdiagnosis and overtreatment of intraosseous venous malformations.

Indexed as

Bone NeoplasmsNFATC Transcription FactorsOncogene Proteins, FusionRibsRNA-Binding Protein EWSSarcomaVascular MalformationsAdolescentDiagnosis, DifferentialHumansMaleSkullSpineEWSR1 protein, humanNFATC Transcription FactorsOncogene Proteins, FusionRNA-Binding Protein EWSEWSR1-NFATC1 fusionintraosseous venous malformationvascular malformation

Identifiers

PMID41960922
PMCPMC13095055

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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.