Evidence map›Paper›PMID 31620852›Full record

ReviewPediatric radiology2019

Overview of the clinical and imaging features of the most common non-rhabdomyosarcoma soft-tissue sarcomas.

Simon C Kao

Abstract readReview
PubMed Publisher
In one paragraph

Review in Pediatric radiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.2field-weighted citation impact, top 18% 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

4 citing papers in PubMed, 16 citations in OpenAlex.

  1. [Pediatric sarcomas].Radiologie (Heidelberg, Germany) · 2026
    Review
  2. Review
  3. Head and neck adult-type soft tissues sarcomas: survival analysis and comparison between the last two editions of the TNM staging system.European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery · 2021
    Article
  4. Synovial Sarcoma: A Clinical Review.Current oncology (Toronto, Ont.) · 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

1 author at 1 institution in 1 country.

Simon C KaoDepartment of Radiology,, University of Iowa Carver College of Medicine,, 200 Hawkins Drive, 3885JPP, Iowa City, IA, 52242, USA. simon-kao@uiowa.edu.ORCID 0000-0002-6843-0555
University of Iowa · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Non-rhabdomyosarcoma soft-tissue sarcoma (NRSTS) refers to a widely heterogeneous group of extraskeletal mesenchymal neoplasms accounting for approximately 4% of all childhood cancers. This article summarizes the clinical and imaging features of these rare tumors and describes in detail the three most common histological types of NRSTSs encountered in children - synovial sarcoma, malignant peripheral nerve sheath tumor and infantile fibrosarcoma. The author discusses the role of non-cross-sectional and cross-sectional imaging.

Indexed as

ChildFibrosarcomaHumansNerve Sheath NeoplasmsRare DiseasesSarcomaSarcoma, SynovialChildrenComputed tomographyMagnetic resonance imagingNon-rhabdomyosarcoma soft-tissue sarcomaOncologyPositron emission tomographyUltrasound

Identifiers

PMID31620852
OpenAlexW2980561890

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.