Sousa Escandón Manuel Alejandro, Mateo Cambón Luis, Pérez Castro-Ellendt Enrique, Pérez Valcarcel Javier, González Rodríguez Alfonso, García Figueiras Roberto
Servicio de Urología Hospital Comarcal de Monforte 27400 Monforte de Lemos, Lugo, España.
Arch Esp Urol. 2002 Mar;55(2):146-52.
To describe two cases of unilateral renal agenesis complicated by the association of a urothelial carcinoma and review the literature.
After reviewing our series of transitional cell carcinoma, we found two cases with associated unilateral renal agenesis. Case 1: A 46-year-old male with grade III stage C transitional cell carcinoma of the urinary bladder that was treated sequentially by transurethral resection of the bladder, systemic neoadjuvant polychemotherapy (gemcitabin, taxol and cisplatin) before radical cystectomy and Bricker urinary diversion were performed. Due to the extent of the tumor, complementary adjuvant therapy was administered, but the patient died 10 months after cystectomy due to disease progression. Case 2: An asymptomatic 71-year-old male in whom renal agenesis and ureteral pelvic filling defect, which was treated by ureterectomy, were incidentally discovered during a routine abdominal study. At one year follow-up, no evidence of tumor recurrence has been observed.
23 patients with unilateral renal agenesis in association with different endocrine or genitourinary cancers have been reported in the literature. In unilateral renal agenesis anomalies of some of the genes involved in renal development occur and may lead to dysplastic growth of the embryologically related organs and an increased risk of developing tumors.
93% of the tumors reported in patients with unilateral renal agenesis were found to arise from the genitourinary organs.
描述两例单侧肾缺如合并尿路上皮癌的病例并复习相关文献。
在回顾我们的移行细胞癌系列病例后,我们发现了两例合并单侧肾缺如的病例。病例1:一名46岁男性,患有膀胱III级C期移行细胞癌,先后接受了经尿道膀胱切除术、根治性膀胱切除术前行全身新辅助多药化疗(吉西他滨、紫杉醇和顺铂)以及Bricker尿流改道术。由于肿瘤范围,给予了辅助性治疗,但患者在膀胱切除术后10个月因疾病进展死亡。病例2:一名71岁无症状男性,在常规腹部检查中偶然发现肾缺如和输尿管肾盂充盈缺损,接受了输尿管切除术。在一年的随访中,未观察到肿瘤复发的证据。
文献报道了23例单侧肾缺如合并不同内分泌或泌尿生殖系统癌症的患者。在单侧肾缺如中,参与肾脏发育的一些基因出现异常,可能导致胚胎相关器官发育异常生长,并增加患肿瘤的风险。
单侧肾缺如患者中报告的肿瘤有93%被发现起源于泌尿生殖器官。