ReviewBMC surgery2020
Primary Ewing's sarcoma in a small intestine - a case report and review of the literature.
Review in BMC surgery, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
What it found
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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.
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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.
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Who cites it
7 citing papers in PubMed, 17 citations in OpenAlex.
- Laparoscopic resection of retro gastric extra osseous Ewing Sarcoma in a 5-year old: a rare case and review of literature.BMC surgery · 2026Review
- Presumptive Ewing Sarcoma of the Jejunum Presenting with Metastatic Disease: A Case Report and Focused Narrative Review.International medical case reports journal · 2026Article
- Primary Extraosseous Ewing sarcoma of the Rectosigmoid region in an adult male: a rare case report.Oxford medical case reports · 2025Article
- Primary Ewing's sarcoma of the intestine: case report and literature review.Frontiers in oncology · 2024Article
- Ewing's sarcoma of the duodenum: a rare clinical condition managed with surgical resection.BMJ case reports · 2023Article
- Ewing sarcoma of the ileum with wide multiorgan metastases: A case report and review of literature.World journal of gastrointestinal oncology · 2022Article
- Ewing Sarcoma/Primitive Neuroectodermal Tumor Involving the Duodenum.Ochsner journal · 2022Article
Corrections and comments
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Authors and funding
6 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundEwing's sarcoma usually presents in paediatric patients with its primary location being bone tissue. Nevertheless, we present such an adult case which arises from the small intestine. We registered thirty one cases of such origin published so far excluding ours. CASE PRESENTATION: We report a case of 30 year old female who was admitted due to the persistent anaemia. Whole body computed tomography scan revealed abdominal mass in her left upper abdominal compartment. Surgery on the mass originating from jejunum was performed, although due to extremely complicated postoperative period and rapid dissemination no additional therapy had been performed. The tumour was positive for CD99, ERG, CD56, Synaptophysin, PanCK, Cam5.2.
conclusionExtraosseus Ewing's sarcoma is extremely rare entity, with poor prognosis.
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Registered trials
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.