囊性肾母细胞瘤,囊性部分分化肾母细胞瘤,还是囊性肾瘤?病例报告及文献回顾

IF 0.4 Q4 UROLOGY & NEPHROLOGY
Renandha Septaryan Yustira , Sean Peter Haruman , Renaningtyas Tambun , Gerhard Reinaldi Situmorang
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引用次数: 0

摘要

肾母细胞瘤是典型的儿童实性肾癌,很少表现为囊性,类似于囊性肾瘤或囊性部分分化肾母细胞瘤。我们报告一个20个月大的男婴表现为右腹部肿块,高血压和食欲不振。MRI显示囊性肾肿瘤,需要不经化疗的原发性肾切除术。术后组织学显示为囊性肾母细胞瘤,需进一步治疗。本病例强调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。手术和化疗策略必须根据临床和影像学结果仔细个性化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cystic wilms tumor, cystic partially differentiated nephroblastoma, or cystic nephroma? A case report and review of the literature
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.
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来源期刊
Urology Case Reports
Urology Case Reports Medicine-Urology
CiteScore
0.90
自引率
20.00%
发文量
325
审稿时长
37 days
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