Evidence map›Paper›PMID 41210564›Full record

ArticleProceedings (Baylor University. Medical Center)2025

Rhabdomyosarcoma with TFCP2 rearrangement in a young adult: a rare case with unique clinical and pathological features.

Hannah Chaudhury, Nicholas Hancock, Jorge Rodriguez Vazquez, Dauod Arif, Genevieve Lapointe, André M Oliveira

Abstract readCase Reports
In one paragraph

Article in Proceedings (Baylor University. Medical Center), 2025. 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

6 authors.

Hannah ChaudhurySchool of Medicine, Texas Tech University Health Sciences Center, Lubbock, Texas, USA.ORCID https://orcid.org/0009-0007-1051-9155
Nicholas HancockSchool of Medicine, Texas Tech University Health Sciences Center, Lubbock, Texas, USA.
Jorge Rodriguez VazquezDepartment of Internal Medicine, Texas Tech University Health Sciences Center, Lubbock, Texas, USA.
Dauod ArifDepartment of Pathology, Texas Tech University Health Sciences Center, Lubbock, Texas, USA.
Genevieve LapointeDepartment of Neurosurgery, Texas Tech University Health Sciences Center, Lubbock, Texas, USA.
André M OliveiraDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Spindle cell rhabdomyosarcoma, a rare subtype of adult soft tissue tumor, is characterized by specific histological and clinical features. This report presents a case of a 21-year-old woman with an intraosseous spindle cell rhabdomyosarcoma in the left frontal region, a less common location in adults. The rarity and atypical presentation of spindle cell rhabdomyosarcoma in adults highlight the importance of thorough histopathological examination and immunohistochemistry in diagnosis. This case emphasizes the complexity of managing such tumors, showcasing the combination of surgical and chemotherapeutic interventions.

Indexed as

Malignant tumorrhabdomyosarcomaspindle cell

Identifiers

PMID41210564
PMCPMC12591595

What OpenQuestion holds

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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.