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首页> 外文期刊>The Journal of Urology >Unilateral multicystic dysplastic kidney with progressive infundibular stenosis in the contralateral kidney: experience at 1 center and review of literature.
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Unilateral multicystic dysplastic kidney with progressive infundibular stenosis in the contralateral kidney: experience at 1 center and review of literature.

机译:对侧肾脏中单侧多囊增生异常性肾脏伴进行性漏斗状狭窄:在1个中心的经验和文献复习。

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PURPOSE: We analyzed the association between unilateral multicystic dysplastic kidney and subsequent contralateral infundibular stenosis, which can result in progressive calyceal dilatation, and has been linked to global hyperfiltration injury and renal impairment. MATERIALS AND METHODS: During the last 10 years 200 children presented with unilateral multicystic dysplastic kidney. Of these children 5 subsequently exhibited contralateral infundibular stenosis. We reviewed the published data on multicystic dysplastic kidney as well as infundibular stenosis to examine this association further. RESULTS: Three patients underwent open surgical exploration since rapid progression with associated parenchymal thinning was detected. Literature review failed to identify any discussion of infundibular stenosis in studies focusing on long-term followup of children with a unilateral multicystic dysplastic kidney. Several case reports and case series discuss this condition in association with other collecting system anomalies. However, these anomalies are hypothesized to be part of a disease spectrum resulting from aberrant formation of the collecting system. Bilateral involvement has been reported in fewer than 10 cases. CONCLUSIONS: Our cases represent a part of the spectrum of pyelocalyceal dysgenesis that can have bilateral involvement of varying degrees. Of particular concern was the delayed presentation in some of our patients and the progressive nature of the lesions. Although exceedingly rare, we wish to highlight the association of multicystic dysplastic kidney and progressive infundibular stenosis of the contralateral kidney and renal impairment.
机译:目的:我们分析了单侧多囊增生异常性肾脏与随后的对侧漏斗状狭窄之间的关联,这可能导致进行性的肾小管扩张,并与整体性超滤损伤和肾脏损害有关。材料与方法:在最近10年中,有200名儿童表现为单侧多囊性增生性肾脏。在这些儿童中,5名随后表现出对侧漏斗状狭窄。我们审查了有关多囊性增生性肾脏以及漏斗状狭窄的已发表数据,以进一步检查这种关联。结果:三名患者进行了开放式外科手术探查,因为检测到了相关的薄壁组织快速变薄。文献综述未能在研究侧重于单侧多囊性增生性肾小儿的长期随访研究中发现任何关于漏斗管狭窄的讨论。一些案例报告和案例系列结合其他收集系统异常情况讨论了这种情况。但是,这些异常被认为是由于收集系统异常形成而导致的疾病谱的一部分。据报道,双边受害不到十例。结论:我们的病例代表了多发性局灶性细胞发育不全的一部分,可双侧受累程度不同。特别令人担忧的是我们的某些患者出现延迟症状以及病变的进行性。尽管极为罕见,但我们希望强调多囊性增生性肾脏与对侧肾脏的进行性漏斗性狭窄和肾脏损害的关系。

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