Evidence map›Paper›PMID 37832362›Full record

ArticleInternational journal of surgery case reports2023

Extraskeletal Ewing's sarcoma of the thigh with lung and bone metastasis: Case report.

Abebaw Muhabaw Zegeye, Birlew T Alemayehu, Degalem Tilahun Worku, Kirubel Addisu Abera, Samuel Addisu Abera, Bewketu Abebe Alemu

Open access · goldAbstract readCase Reports
In one paragraph

Article in International journal of surgery case reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.8field-weighted citation impact, top 24% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
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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 at 1 institution in 1 country.

Abebaw Muhabaw ZegeyeDepartment of Orthopedics, University of Gondar, College of Medicine and Health Sciences, Gondar, Ethiopia. Electronic address: yeabm3@gmail.com.
Birlew T AlemayehuDepartment of Orthopedics, University of Gondar, College of Medicine and Health Sciences, Gondar, Ethiopia.
Degalem Tilahun WorkuDepartment of Pediatrics, University of Gondar, College of Medicine and Health Sciences, Gondar, Ethiopia.
Kirubel Addisu AberaDepartment of Pathology, University of Gondar, College of Medicine and Health Sciences, Gondar, Ethiopia.
Samuel Addisu AberaDepartment of Pathology, University of Gondar, College of Medicine and Health Sciences, Gondar, Ethiopia.
Bewketu Abebe AlemuDepartment of Pathology, University of Gondar, College of Medicine and Health Sciences, Gondar, Ethiopia.
University of Gondar · ET

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introduction and importanceExtraskeletal Ewing's sarcoma is an uncommon tumor with a devastating prognosis and a very high mortality rate, particularly in metastatic forms, it primarily affects young people mainly in the 2nd to 4th decades of life. It can affect different parts of the body, without a particular clinical presentation which delays diagnosis. CASE PRESENTATION: 12-year-old male patient presented with swelling over the left proximal thigh of 7 months duration associated with pain and limping. On physical examination, he had about 20 × 15 cm firm, tender, and erythematous proximal left thigh swelling that is fixed to the structures with an overlying scar. CLINICAL DISCUSSION: Extra skeletal Ewing's sarcoma (EES) is a member of the Ewing Sarcoma Family of tumors. EES is a rare tumor with an incidence ranging from 0.1 to 0.4 per a million people. It presented with rapidly increasing swelling mainly over the soft tissue of the proximal thigh, pelvis, paravertebral region, chest wall, upper arm and shoulder. Age at presentation ranges 10 to 30 years with no gender preference. Imaging is crucial in the diagnosis, preoperative assessment, in staging and evaluation of treatment outcomes. Histopathology study is mandatory for the definitive diagnosis of EES among competitive differential diagnoses. The management of EES includes Surgery, chemotherapy and/or radiation therapy based on the stage of the disease.

conclusionEES is a rare tumor but it should be in the differential diagnosis of adolescent patients presented with soft tissue mass/swelling.

Indexed as

Case reportEwing's sarcomaExtraskeletalLungMetastasis

Identifiers

PMID37832362
PMCPMC10667788
OpenAlexW4387345208

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.