Al-Gburi Saleh, Thonse Vinutha, Abdalla Omer, Kumar Manal
Urology, Arrowe Park Hospital, Wirral University Teaching Hospital NHS Foundation Trust, Wirral, GBR.
Urology, Mosul Medical College, University of Mosul, Mosul, IRQ.
Cureus. 2024 Feb 9;16(2):e53916. doi: 10.7759/cureus.53916. eCollection 2024 Feb.
Ewing's sarcoma is generally observed in the skeletal and connective tissues of paediatric individuals. The occurrence of extraosseous neuroectodermal tumours is uncommon. Renal Ewing's sarcoma usually presents with flank pain, haematuria, or as an abdominal mass. Immunohistochemistry and fluorescence in situ hybridization (FISH) techniques are essential in its diagnosis and differentiation from other tumours. We present asymptomatic renal Ewing's sarcoma in a 19-year-old female patient who was diagnosed incidentally, and the CT scan confirmed a 2.8 cm left mid-pole renal mass suggestive of malignancy. She was managed with a robotic partial nephrectomy. Tumour immunohistochemistry and the FISH technique confirmed the diagnosis of Ewing's sarcoma. The patient made an uneventful recovery and was referred for chemotherapy. This case report illustrates that despite the aggressiveness of the tumour, it can be detected earlier despite an asymptomatic presentation and be successfully treated with nephron-sparing surgery and chemotherapy.
尤因肉瘤通常见于小儿的骨骼和结缔组织。骨外神经外胚层肿瘤的发生并不常见。肾尤因肉瘤通常表现为胁腹痛、血尿或腹部肿块。免疫组织化学和荧光原位杂交(FISH)技术对其诊断以及与其他肿瘤的鉴别至关重要。我们报告了一名19岁女性患者的无症状肾尤因肉瘤,该患者为偶然诊断,CT扫描证实左肾中极有一个2.8 cm的肾肿块,提示为恶性肿瘤。她接受了机器人辅助部分肾切除术。肿瘤免疫组织化学和FISH技术确诊为尤因肉瘤。患者恢复顺利,并被转诊接受化疗。本病例报告表明,尽管肿瘤具有侵袭性,但即使无症状表现也可早期发现,并通过保留肾单位手术和化疗成功治疗。