首页> 外文期刊>The Journal of Urology >Fibroepithelial polyps causing ureteropelvic junction obstruction in children.
【24h】

Fibroepithelial polyps causing ureteropelvic junction obstruction in children.

机译:纤维上皮息肉引起小儿输尿管盂连接处阻塞。

获取原文
获取原文并翻译 | 示例
       

摘要

PURPOSE: Fibroepithelial polyps are benign mucosal projections that can be found throughout the urinary system. We review our experience with fibroepithelial polyps of the ureteropelvic junction in children to define more clearly this entity and its outcome following treatment. METHODS: We reviewed the records of all children with fibroepithelial polyps causing ureteropelvic junction obstruction treated at our institution between December 1967 and February 2002. RESULTS: Nine patients 6 weeks to 9 years old had 11 ureteropelvic junction obstructions secondary to fibroepithelial polyps, representing a 0.5% incidence of all ureteropelvic junction obstructions seen during that period. The majority of the patients were male (89%) and had obstruction on the left side (78%). Only 22% of the patients had a diagnosis of obstructing polyps suggested preoperatively. All patients underwent dismembered pyeloplasty but 1 required subsequent nephrectomy due to progressive loss of renal function. All lesions were characterized microscopically by polypoid projections of fibrous tissue covered by epithelium and demonstrating varying degrees of inflammation. No recurrences were seen during a mean followup of 44 months. CONCLUSIONS: Fibroepithelial polyps are rare lesions that cause ureteropelvic junction obstruction in children, primarily in males and on the left side. Filling defects were diagnosed preoperatively in 22% of the patients in this series. Excision and dismembered pyeloplasty were curative, and recurrences were not observed. The etiology of this disease remains obscure.
机译:目的:纤维上皮息肉是在整个泌尿系统中都可见的良性粘膜突起。我们回顾了儿童输尿管骨盆连接处纤维上皮息肉的经验,以更明确地定义该实体及其治疗后的结局。方法:我们回顾了1967年12月至2002年2月间在本院接受治疗的所有引起上输尿管盆腔连接阻塞的纤维上皮息肉患儿的记录。结果:9例6周至9岁的患者有11例继发于纤维上皮息肉的输尿管​​盆腔阻塞,占0.5%在此期间看到的所有输尿管盆腔连接阻塞的发生率%。大多数患者为男性(89%),左侧有梗阻(78%)。仅有22%的患者术前建议诊断为息肉阻塞。所有患者均接受了肢解性肾盂成形术,但由于肾功能进行性丧失,因此有1位患者需要进行随后的肾切除术。在显微镜下,所有病变的特征是上皮覆盖的纤维组织的息肉状突起,表现出不同程度的炎症。平均随访44个月未见复发。结论:纤维上皮息肉是罕见的病变,可引起儿童输尿管骨盆连接处梗阻,主要在男性和左侧。在本系列中有22%的患者术前诊断出充盈缺损。根治术和肢体切除均能治愈,且未见复发。该病的病因仍不清楚。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号