ArticleOxford medical case reports2025
Primary Extraosseous Ewing sarcoma of the Rectosigmoid region in an adult male: a rare case report.
Article in Oxford medical case reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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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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6 authors.
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Abstract
backgroundEwing sarcoma rarely arises in the gastrointestinal (GI) tract, and rectosigmoid presentations are exceptionally uncommon. CASE PRESENTATION: 36-year-old man with rectosigmoid mass showing small round blue cells with pseudorosettes, CD99 and FLI1 positive, diagnosed as Ewing sarcoma; managed with surgical resection followed by chemotherapy.
conclusionPrimary EES of rectosigmoid is extremely rare; diagnosis requires morphology, IHC and molecular testing wherever possible; early biopsy allows neoadjuvant chemo before surgery.
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