Department of Pediatric Surgery, XinHua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, 1665, Kongjiang Road, Shanghai 200092, PR China.
World J Surg Oncol. 2013 May 20;11:102. doi: 10.1186/1477-7819-11-102.
Here, we report a new case of botryoid Wilms' tumor, a 4-year-old boy, who was referred to us with a chief complaint of dysuria and gross hematuria. The computed tomography and radical nephroureterectomy showed that a botryoid sarcoma-like appearance occupied the right renal pelvis and extended into the bladder. Histologic examination further confirmed this case was a mixed type of Wilms' tumor. In a word, we demonstrated a rare case of botryoid Wilms' tumor, which extended from the renal pelvis into the ureter and bladder, then some degenerative and necrotic tissue with calcification discharged from urethra. Postoperative adjuvant chemotherapy was executed. At 24-month follow-up, there was no evidence of recurrence.
在这里,我们报告了一例新的类癌型肾母细胞瘤病例,这是一名 4 岁男孩,因尿痛和肉眼血尿就诊。计算机断层扫描和根治性肾输尿管切除术显示,类癌样外观的肉瘤样肿块占据了右肾盂并延伸至膀胱。组织学检查进一步证实了这例为混合性肾母细胞瘤。总之,我们展示了一例罕见的从肾盂延伸至输尿管和膀胱的类癌型肾母细胞瘤,随后从尿道排出一些退行性和坏死组织伴钙化。术后辅助化疗。在 24 个月的随访中,没有复发的迹象。