ArticleThe Permanente journal2019
Extraskeletal Ewing Sarcoma of the Jejunum: A Case Report.
Article in The Permanente journal, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
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Who cites it
9 citing papers in PubMed, 12 citations in OpenAlex.
- Presumptive Ewing Sarcoma of the Jejunum Presenting with Metastatic Disease: A Case Report and Focused Narrative Review.International medical case reports journal · 2026Article
- Primary Ewing's sarcoma of the intestine: case report and literature review.Frontiers in oncology · 2024Article
- Ewing sarcoma of the ileum with wide multiorgan metastases: A case report and review of literature.World journal of gastrointestinal oncology · 2022Article
- Imaging-based diagnosis for extraskeletal Ewing sarcoma in pediatrics: A case report.World journal of clinical cases · 2022Article
- Article
- Challenges of Diagnosing Primary Ewing's Sarcoma in the Small Intestine of the Elderly: A Case Report.Frontiers in oncology · 2021Article
- Primary Ewing's sarcoma in a small intestine - a case report and review of the literature.BMC surgery · 2020Review
- Case Report: Primary Ewing Sarcoma of the Penis With Multiple Metastases.Frontiers in pediatrics · 2020Article
- Ewing Sarcoma With Emphasis on Extra-skeletal Ewing Sarcoma: A Decade's Experience From a Single Centre in India.Clinical pathology (Thousand Oaks, Ventura County, Calif.)Article
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Authors and funding
4 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
introductionEwing sarcoma most commonly arises in bones but rarely presents in extraskeletal locations. We report one such case arising from the jejunum. CASE PRESENTATION: A 67-year-old woman presented with acute-onset, right lower quadrant pain. Computed tomography results showed a large mass within the midjejunum with pneumoperitoneum. Surgical excision was performed, and an extraskeletal Ewing sarcoma of the jejunum was suspected histologically. The diagnosis was confirmed with fluorescence in situ hybridization studies.
conclusionThis case emphasizes the importance of recognizing this rare presentation in the small intestine to broaden the differential diagnosis of adult intraabdominal tumors.
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