Evidence map›Paper›PMID 36646985›Full record

ArticleHead and neck pathology2023

A Low-grade Sinonasal Sarcoma Harboring EWSR1::BEND2: Expanding the Differential Diagnosis of Sinonasal Spindle Cell Neoplasms.

Doreen N Palsgrove, Varsha Manucha, Jason Y Park, Justin A Bishop

Open access · greenAbstract readCase Reports
In one paragraph

Article in Head and neck pathology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
4.1field-weighted citation impact, top 6% of its field
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

11 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. A pediatric low-grade sinonasal mesenchymal tumor harboring a novel CHD9::BEND2 fusion.Virchows Archiv : an international journal of pathology · 2025
    Article
  3. Review
  4. Article
  5. Article
  6. EWSR1::BEND2 fusion sarcoma in bone: a report of two rare cases.Virchows Archiv : an international journal of pathology · 2025
    Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Identification of Novel/RareInternational journal of molecular sciences · 2024
    Article
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

4 authors at 3 institutions in 1 country.

Doreen N PalsgroveDepartment of Pathology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Varsha ManuchaDepartment of Pathology, University of Mississippi Medical Center, Jackson, MS, USA.
Jason Y ParkDepartment of Pathology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Justin A BishopDepartment of Pathology, University of Texas Southwestern Medical Center, Dallas, TX, USA. Justin.Bishop@UTSouthwestern.edu.ORCID http://orcid.org/0000-0002-9743-4360
The University of Texas Southwestern Medical Center · USJackson Memorial Hospital · USSouthwestern Medical Center · US

Funding

Jane B. and Edwin P. Jenevein M.D Endowment for Pathology at UT Southwestern Medical Center Jane B. and Edwin P. Jenevein M.D Endowment for Pathology at UT Southwestern Medical Center
6 · The paper itself

Abstract

backgroundMolecular diagnostics has greatly refined sinonasal tumor pathology over the past decade. While much of the attention has focused on carcinomas, it is becoming clear that there are emerging mesenchymal neoplasms which have previously defied classification.

methodsHere, we present a 33-year-old woman with a multiply recurrent sinonasal spindle cell tumor exhibiting distinctive features, and not easily classifiable into a specific category.

resultsThe hypercellular tumor was composed of plump spindled cells, with uniform vesicular chromatin arranged as vague fascicles around a prominent hemangiopericytoma-like vasculature. The mitotic rate was brisk at 10 per 10 high power fields. By immunohistochemistry, it was only positive for EMA (focal) and SATB2 (diffuse, weak). Fusion analysis uncovered EWSR1::BEND2, a fusion which is best known for being seen in astroblastoma, but which has not yet been reported in sarcomas.

conclusionThis case underscores the utility of fusion analysis when confronted with a sinonasal spindle cell neoplasm which does not neatly fit into any specific category. It remains to be seen if EWSR1::BEND2 sinonasal sarcoma represents a distinct entity.

Indexed as

Paranasal Sinus NeoplasmsSarcomaSoft Tissue NeoplasmsAdultBiomarkers, TumorDiagnosis, DifferentialFemaleHumansRNA-Binding Protein EWSTranscription FactorsBiomarkers, TumorEWSR1 protein, humanRNA-Binding Protein EWSTranscription FactorsEWSR1:BEND2Molecular diagnosticsSarcomaSinonasal tract

Identifiers

PMID36646985
PMCPMC10293148
OpenAlexW4316511420

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.