首页> 外文期刊>The Journal of Urology >Nephron Sparing Surgery for Unilateral Wilms Tumor in Children with Predisposing Syndromes: Single Center Experience Over 10 Years
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Nephron Sparing Surgery for Unilateral Wilms Tumor in Children with Predisposing Syndromes: Single Center Experience Over 10 Years

机译:有易感综合征的儿童单侧肾盂肿瘤的肾保留手术:10年以上的单中心经验

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Purpose: Unilateral Wilms tumors associated with predisposing syndromes are treated with preoperative chemotherapy followed by surgical resection. We describe our experience with nephron sparing surgery for Wilms tumor in this population at risk for metachronous lesions.Materials and Methods: We conducted a retrospective review of all children with a predisposing syndrome who underwent nephrectomy for malignancy during a 10-year period (2000 to 2010). Data collected included age, mode of detection, tumor size, treatment, pathology results, followup time and recurrence episodes. Results: From 2000 to 2010, 13 of 75 (19%) patients treated for Wilms tumor were diagnosed with predisposing syndrome(s). Eight patients with unilateral tumors were treated and had a mean age at diagnosis of 27 months (range 7 months to 9 years). Beckwith-Wiedemann syndrome, isolated hemihyperplasia, WAGR (Wilms tumor, Aniridia, Genitourinary abnormalities, mental Retardation) syndrome and isolated lip 13 deletion were the underlying diagnoses in 3, 2, 2 and 1 patient, respectively. All but 2 patients were diagnosed by screening ultrasound and 5 underwent preoperative chemotherapy. Median tumor size at surgery was 2.5 cm (range 1 to 13). Nephron sparing surgery was performed in 6 of 8 patients. Pathological study showed favorable histology Wilms tumor and nephrogenic rests in 6 and 2 patients, respectively. After a mean followup of 36 months (range 6 to 72) no recurrences were documented and all children had normal creatinine levels.Conclusions: Nephron sparing surgery appears safe for patients with unilateral Wilms tumor associated with predisposing syndrome(s), allowing for the preservation of renal function and good oncologic outcomes for the available followup time. If more studies confirm our observation, current recommendations for the surgical treatment of Wilms tumor may need to reemphasize the value of attempting nephron sparing surgery in this patient population.
机译:目的:与易感综合征相关的单侧Wilms肿瘤通过术前化学疗法治疗,然后进行手术切除。我们描述了在该人群中发生肾损伤的Wilms肿瘤保留肾外科手术的经验。材料和方法:我们对所有患有易感综合征的儿童进行了10年(2000年至2000年2010)。收集的数据包括年龄,检测方式,肿瘤大小,治疗,病理结果,随访时间和复发发作。结果:从2000年到2010年,在接受Wilms肿瘤治疗的75名患者中,有13名(19%)被诊断出患有易感综合征。治疗了八例单侧肿瘤患者,诊断时平均年龄为27个月(7个月至9岁)。 Beckwith-Wiedemann综合征,孤立的半身增生,WAGR(威尔姆斯肿瘤,无虹膜,泌尿生殖系统异常,智力低下)综合征和孤立的13号唇缺失分别是3、2、2和1例患者的基础诊断。除2例患者外,所有患者均通过超声检查确诊,其中5例接受了术前化疗。手术时肿瘤的中位大小为2.5 cm(范围1至13)。 8例患者中有6例进行了肾盂保留手术。病理学研究显示,分别有6例和2例患者的组织学研究结果显示,Wilms肿瘤和肾源性息肉息息相关。平均随访36个月(范围6到72),未发现复发,所有儿童的肌酐水平均正常。在可用的随访时间内检查肾功能和良好的肿瘤学结局。如果更多的研究证实了我们的观察结果,那么当前针对Wilms肿瘤进行手术治疗的建议可能需要在该患者人群中再次强调尝试行肾保留肾手术的价值。

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