Yustira Renandha Septaryan, Haruman Sean Peter, Tambun Renaningtyas, Situmorang Gerhard Reinaldi
Department of Urology, St. Carolus Hospital, Jakarta, Indonesia.
Department of Pathological Anatomy, St. Carolus Hospital, Jakarta, Indonesia.
Urol Case Rep. 2025 Aug 31;63:103186. doi: 10.1016/j.eucr.2025.103186. eCollection 2025 Nov.
Wilms tumor, typically a solid pediatric kidney cancer, can rarely appear cystic, mimicking cystic nephroma or cystic partially differentiated nephroblastoma. We report a 20-month-old boy presented with a right abdominal mass, hypertension, and poor appetite. MRI showed a cystic renal tumor, requiring primary nephrectomy without chemotherapy. Postoperative histology revealed a cystic Wilms tumor, necessitating further treatment. This case highlights the diagnostic challenge of cystic renal tumors and emphasizes the importance of histopathology in guiding management. Surgical and chemotherapeutic strategies must be carefully individualized based on clinical and imaging findings.
肾母细胞瘤通常是一种小儿实性肾癌,很少会呈囊性,类似囊性肾瘤或囊性部分分化性肾母细胞瘤。我们报告一名20个月大的男孩,出现右腹部肿块、高血压和食欲不佳。磁共振成像显示为囊性肾肿瘤,需要在不进行化疗的情况下进行一期肾切除术。术后组织学检查显示为囊性肾母细胞瘤,需要进一步治疗。该病例突出了囊性肾肿瘤的诊断挑战,并强调了组织病理学在指导治疗中的重要性。必须根据临床和影像学检查结果仔细制定个体化的手术和化疗策略。