Evidence map›Paper›PMID 32710151›Full record

ArticleSkeletal radiology2021

EWSR1-SMAD3 fibroblastic tumour of bone: expanding the clinical spectrum.

Solange De Noon, Adrienne M Flanagan, Roberto Tirabosco, Paul O'Donnell, Fernanda Amary

Abstract readCase Reports
PubMed Publisher
In one paragraph

Article in Skeletal radiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Frontiers in oncology · 2022
    Article
  6. Diagnostics (Basel, Switzerland) · 2021
    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

5 authors at 2 institutions in 1 country.

Solange De NoonDepartment of Histopathology, Royal National Orthopaedic Hospital, Stanmore, Greater London, UK.
Adrienne M FlanaganDepartment of Histopathology, Royal National Orthopaedic Hospital, Stanmore, Greater London, UK.
Roberto TiraboscoDepartment of Histopathology, Royal National Orthopaedic Hospital, Stanmore, Greater London, UK.
Paul O'DonnellDepartment of Radiology, Royal National Orthopaedic Hospital, Stanmore, UK.
Fernanda AmaryDepartment of Histopathology, Royal National Orthopaedic Hospital, Stanmore, Greater London, UK. Fernanda.amary@nhs.net.
University College London · GBRoyal National Orthopaedic Hospital · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

EWSR1-SMAD3 fibroblastic tumour is a recently described soft tissue lesion. To date, eight cases have been reported, all sited in superficial soft tissue, typically occurring in the hands and feet with a tendency for local recurrence if incompletely excised. No metastatic spread has been reported, and hence, these tumours are currently considered benign. Herein, we present the radiological and histological features of the first reported occurrence of this entity in bone: a 44-year-old man with a tumour in the right tibia, treated with en bloc resection and showing no signs of relapse at 7 years. This tumour should be added to the differential diagnosis of bone lesions which harbour EWSR1 gene rearrangement.

Indexed as

Calmodulin-Binding ProteinsRNA-Binding ProteinsAdultHumansMaleRNA-Binding Protein EWSSmad3 ProteinCalmodulin-Binding ProteinsEWSR1 protein, humanRNA-Binding Protein EWSRNA-Binding ProteinsSmad3 ProteinSMAD3 protein, humanBone tumourEWSR1EWSR1-SMAD3SarcomaTumour

Identifiers

PMID32710151
OpenAlexW3045224138

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.