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单侧多囊性发育不良肾伴对侧肾漏斗部进行性狭窄:1 中心经验及文献复习。

Unilateral multicystic dysplastic kidney with progressive infundibular stenosis in the contralateral kidney: experience at 1 center and review of literature.

机构信息

Sydney Children's Hospital Randwick, Sydney, Australia.

出版信息

J Urol. 2011 Sep;186(3):1053-8. doi: 10.1016/j.juro.2011.05.001. Epub 2011 Jul 23.

DOI:10.1016/j.juro.2011.05.001
PMID:21784480
Abstract

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.

摘要

目的

我们分析了单侧多囊性发育不良肾与随后对侧漏斗部狭窄的关系,后者可导致肾盏进行性扩张,并与全球高滤过性损伤和肾功能损害有关。

材料与方法

在过去的 10 年中,有 200 名儿童出现单侧多囊性发育不良肾。其中 5 例随后出现对侧漏斗部狭窄。我们回顾了多囊性发育不良肾和漏斗部狭窄的已发表数据,以进一步研究这种相关性。

结果

由于发现快速进展伴实质变薄,有 3 例患者接受了开放手术探查。文献复习未能在专注于单侧多囊性发育不良肾儿童长期随访的研究中发现任何关于漏斗部狭窄的讨论。有几个病例报告和病例系列讨论了这种情况与其他集合系统异常有关。然而,这些异常被假设是由于集合系统异常形成导致的疾病谱的一部分。双侧受累的病例少于 10 例。

结论

我们的病例代表了肾盂肾盏发育不良谱的一部分,其双侧受累程度不同。特别值得关注的是我们一些患者的延迟表现和病变的进行性特征。尽管极为罕见,但我们希望强调多囊性发育不良肾与对侧肾漏斗部进行性狭窄和肾功能损害的相关性。

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