Evidence map›Paper›PMID 41938423›Full record

ArticleInternational journal of surgery case reports2026

Primary Ewing Sarcoma of the urinary bladder in an adolescent: a case report of successful organ preservation with multimodal therapy.

Murad Ahmad Al Hasan, Naji Abdoush, Khaled Ghanem

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Article in International journal of surgery case reports, 2026. 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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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Murad Ahmad Al HasanDepartment of Urology, Al-Bairouni University Hospital, Damascus University, Damascus, Syria.ORCID https://orcid.org/0009-0005-2010-1700
Naji AbdoushDepartment of Urology, Al-Bairouni University Hospital, Damascus University, Damascus, Syria.
Khaled GhanemBASMA Pediatric Oncology Unit, Al-Bairouni University Hospital, Damascus University, Damascus, Syria.ORCID https://orcid.org/0000-0002-3601-2244

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction and importance: Primary bladder sarcomas, particularly Ewing Sarcoma/primitive neuroectodermal tumor (ES/PNET), are exceptionally rare in the pediatric and adolescent population, presenting diagnostic and therapeutic challenges. Case presentation: A 15-year-old Syrian girl from a rural area, presented with lower abdominal pain and gross hematuria. Examination revealed suprapubic tenderness. Computed tomography identified a bladder dome mass and a subsequent image-guided biopsy confirmed ES/PNET. The patient received eight cycles of neoadjuvant chemotherapy, which led to significant regression on post-chemotherapy magnetic resonance imaging. Partial cystectomy with 2-cm margins was performed, followed by primary bladder closure. Pathology confirmed pathological complete response, showing no viable tumor (inflammatory changes, urothelial hyperplasia, necrosis, and fibrosis). Adjuvant radiotherapy was administered, and the patient is currently completing adjuvant chemotherapy. Surveillance imaging and cystoscopy 2 months post-operatively showed no evidence of recurrent disease. Clinical discussion: The rarity of bladder ES/PNET presents a therapeutic challenge. This case aligns with emerging evidence that neoadjuvant chemotherapy can be highly effective, facilitating less radical surgery. This strategy successfully avoided radical cystectomy, thereby preventing the associated long-term complications of urinary diversion. The addition of adjuvant radiotherapy was motivated by the initial presence of extensive soft tissue invasion and borderline lymph nodes, aiming to optimize local control. Conclusion: Multimodal therapy with neoadjuvant chemotherapy followed by adjuvant chemotherapy and radiotherapy can facilitate bladder preservation in pediatric bladder ES/PNET without compromising oncological outcomes. This strategy can mitigate the long-term morbidity of radical surgery.

Indexed as

bladder sarcomascase reportEwing Sarcomaorgan preservationpartial cystectomy

Identifiers

PMID41938423
PMCPMC13045995

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