...
首页> 外文期刊>Indian Journal of Urology: IJU: Journal of the Urological Society of India >Renal dysplasia with single system ectopic ureter: Diagnosis using magnetic resonance urography and management with laparoscopic nephroureterectomy in pediatric age
【24h】

Renal dysplasia with single system ectopic ureter: Diagnosis using magnetic resonance urography and management with laparoscopic nephroureterectomy in pediatric age

机译:单系统异位输尿管肾发育不良:小儿年龄段的磁共振尿路造影诊断及腹腔镜肾结石切除术的处理

获取原文
   

获取外文期刊封面封底 >>

       

摘要

Single system ureteral ectopia and associated congenital dysplastic kidney is surgically curable etiology of incontinence with other wise normal pattern of voiding in female child. We share our experience of eight cases in last one year and its management with laparoscopic nephroureterectomy at a tertiary care hospital in India which is one of the largest series in such a short duration of this rare anomaly.Materials and Methods:Patients presented with clinical features of continence with otherwise normal pattern of voiding were clinically examined and investigated by ultrasound (USG), nuclear renal scan, magnetic resonance urography (MRU). Laparoscopic nephroureterectomy was done in all the eight cases and renal dysplasia was confirmed on histological examination.Results:All the patients were females in the age group of five months to five years. USG detected the renal dysplasia in three out of eight cases; however, it could not detect the course of the ectopic ureter in any of the cases. MRU picked up the dysplastic moieties and their location as well as functional status and also depicted the course of the ectopic ureter opening into the vaginal wall in all the eight cases. Laparoscopic nephroureterectomy was done in all the cases and patients were cured off their symptoms.Conclusion:Single system ectopic ureter associated with congenital renal dysplasia is exceedingly rare. MRU is definitely the better investigation for the diagnosis of this condition as compared to the conventional radiological investigations. Laparoscopic nephroureterectomy is a very good procedure for the management of these cases.
机译:单系统输尿管外翻和相关的先天性增生性肾脏是可手术治疗的尿失禁病因,并伴有其他正常的女性排尿方式。我们在过去的一年中分享了我们在八例病例中的经验以及在印度三级医院的腹腔镜肾结石切除术治疗方面的经验,这是在这种罕见异常情况如此短的时间内最大的系列病例之一。材料和方法:具有临床特征的患者临床上已通过超声(USG),核肾扫描,核磁共振尿路造影(MRU)检查并调查了正常排尿方式的排尿障碍。 8例均行腹腔镜肾结石切除术,经组织学检查证实为肾发育不良。结果:5例〜5岁年龄段均为女性。 USG在八分之三的病例中发现了肾脏发育异常;但是,在任何情况下都无法检测到异位输尿管的走向。 MRU记录了这8例病例中异常增生的部分,它们的位置以及功能状态,还描绘了异位输尿管向阴道壁开放的过程。所有病例均行腹腔镜肾结直肠癌切除术,患者的症状得到治愈。结论:单系统异位输尿管伴有先天性肾发育不良的情况极为罕见。与常规放射学检查相比,MRU绝对是诊断这种疾病的更好检查方法。腹腔镜肾切除术是处理这些病例的非常好的方法。

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