Evidence map›Paper›PMID 41835741›Full record

ArticleCureus2026

Soft Tissue Ewing Sarcoma in a Child: A Rare Localization.

Larbi Benradi, Hanane Salhi, Mohamed Belahcen

Abstract readCase Reports
In one paragraph

Article in Cureus, 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

3 authors.

Larbi BenradiPediatric Surgery, Mohammed VI University Hospital of Oujda, Oujda, MAR.
Hanane SalhiPediatric Surgery, CHU Mohammed VI, Oujda, MAR.
Mohamed BelahcenPediatric Surgery, Mohammed VI University Hospital of Oujda, Oujda, MAR.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ewing sarcoma (ES) is a primitive neuroectodermal tumor usually located in the bones. The soft tissue as a primary localisation of ES is extremely rare. A few cases have been reported in the literature; the most affected areas are the head, trunk, neck, upper and lower limbs, or even multiple lesions. It is most often a painful and mobile subcutaneous swelling with a soft consistency; metastasis is very rare. Differential diagnosis is made with other small round cell neoplasms. Therapy for ES includes chemotherapy, radiation therapy, and surgery. In this paper, we discuss the findings of a soft tissue ewing sarcoma (STES) located in the right arm in a 14-year-old boy successfully treated in our department of pediatric surgery. The follow-up did not show any sign of recurrence after 24 months.

Indexed as

childewing sarcomamultidisciplinarysoft tissuesurgery

Identifiers

PMID41835741
PMCPMC12981967

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.