• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

产前检测到的多囊性发育不良肾的超声进展

Ultrasound progression of prenatally detected multicystic dysplastic kidney.

作者信息

Siqueira Rabelo Eli A, Oliveira Eduardo A, Silva Jose Maria P, Oliveira Daniely S, Colosimo Enrico A

机构信息

Department of Pediatrics, Pediatric Nephrourology Unit, Hospital das Clínicas, Federal University of Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.

出版信息

Urology. 2006 Nov;68(5):1098-102. doi: 10.1016/j.urology.2006.06.004. Epub 2006 Nov 7.

DOI:10.1016/j.urology.2006.06.004
PMID:17095058
Abstract

OBJECTIVES

To evaluate the sonographic involution of prenatally detected multicystic dysplastic kidney (MCDK).

METHODS

A total of 53 children with unilateral MCDK detected by prenatal ultrasonography between 1989 and 2004 were included in this analysis. All children received conservative management with follow-up visits every 6 months. Follow-up ultrasound examinations were performed at 6-month intervals during the first 2 years after birth and yearly thereafter. A linear mixed effect model was constructed, including MCDK length as the dependent variable and body size parameters and contralateral renal dimensions as independent variables.

RESULTS

The mean follow-up time was 68 months. A total of 334 ultrasound scans were analyzed. The ultrasound scan demonstrated partial or total involution of the MCDK in 48 cases (91%). A consistent negative correlation was found among MCDK length, patient age, and body size parameters. As a whole, the MCDK length reduction was estimated to be 0.29 mm/mo. The rate of reduction was not constant over time and was intense during the first 30 months of age. According to the regression model, MCKD reduced in length by 0.80 mm/mo during the first 30 months of age, 0.26 mm between 30 and 84 months old, and 0.30 mm in children older than 84 months.

CONCLUSIONS

Our results suggest a clear tendency of MCDK to decrease in size, with the rate of the involution greater during the first 30 months than the rate in older children.

摘要

目的

评估产前检测到的多囊性发育不良肾(MCDK)的超声消退情况。

方法

本分析纳入了1989年至2004年间经产前超声检查发现的53例单侧MCDK患儿。所有患儿均接受保守治疗,每6个月进行一次随访。出生后的前2年每6个月进行一次随访超声检查,此后每年进行一次。构建了一个线性混合效应模型,将MCDK长度作为因变量,身体大小参数和对侧肾脏尺寸作为自变量。

结果

平均随访时间为68个月。共分析了334次超声扫描。超声扫描显示48例(91%)的MCDK部分或完全消退。在MCDK长度、患儿年龄和身体大小参数之间发现了一致的负相关。总体而言,MCDK长度减少估计为每月0.29毫米。减少率随时间并非恒定不变,在30个月龄前较为明显。根据回归模型,MCKD在30个月龄前长度每月减少0.80毫米,在30至84个月龄之间减少0.26毫米,在84个月龄以上的儿童中减少0.30毫米。

结论

我们的结果表明MCDK有明显的尺寸减小趋势,其消退率在30个月龄前比大龄儿童更高。

相似文献

1
Ultrasound progression of prenatally detected multicystic dysplastic kidney.产前检测到的多囊性发育不良肾的超声进展
Urology. 2006 Nov;68(5):1098-102. doi: 10.1016/j.urology.2006.06.004. Epub 2006 Nov 7.
2
[Conservative management of multicystic dysplastic kidney: clinical course and ultrasound outcome].多囊性发育不良肾的保守治疗:临床过程及超声检查结果
J Pediatr (Rio J). 2005 Sep-Oct;81(5):400-4. doi: 10.2223/JPED.1391.
3
Natural history of multicystic kidney conservatively managed: a prospective study.多囊肾保守治疗的自然病史:一项前瞻性研究。
Pediatr Nephrol. 2004 Oct;19(10):1102-7. doi: 10.1007/s00467-004-1549-2. Epub 2004 Jul 16.
4
Predictive factors of ultrasonographic involution of prenatally detected multicystic dysplastic kidney.产前检测到的多囊性发育不良肾超声消退的预测因素。
BJU Int. 2005 Apr;95(6):868-71. doi: 10.1111/j.1464-410X.2005.05418.x.
5
Unilateral multicystic dysplastic kidney: experience in children.单侧多囊性发育不良肾:儿童病例经验
BJU Int. 2004 Feb;93(3):388-92. doi: 10.1111/j.1464-410x.2003.04623.x.
6
Unilateral multicystic dysplastic kidney: does initial size matter?单侧多囊性发育不良肾:初始大小是否重要?
Pediatr Nephrol. 2012 Aug;27(8):1335-40. doi: 10.1007/s00467-012-2141-9. Epub 2012 Mar 13.
7
The natural history of the multicystic dysplastic kidney--is limited follow-up warranted?多囊性发育不良肾的自然病史——有限的随访是否必要?
J Pediatr Urol. 2014 Aug;10(4):655-61. doi: 10.1016/j.jpurol.2014.06.001. Epub 2014 Jul 4.
8
Ultrasound diagnosis of multicystic dysplastic kidney: is a confirmatory nuclear medicine scan necessary?多囊性发育不良肾的超声诊断:是否需要进行确诊性核医学扫描?
J Pediatr Urol. 2014 Dec;10(6):1059-62. doi: 10.1016/j.jpurol.2014.03.011. Epub 2014 May 2.
9
MCDK not excluded by virtue of function on renal scan.肾扫描功能不排除多囊性发育不良肾。
Can J Urol. 2002 Dec;9(6):1690-3.
10
Multicystic dysplastic kidney: Impact of imaging modality selection on the initial management and prognosis.多囊性发育不良肾:成像方式选择对初始治疗及预后的影响。
J Pediatr Urol. 2014 Aug;10(4):645-9. doi: 10.1016/j.jpurol.2014.03.004. Epub 2014 Mar 29.

引用本文的文献

1
Multicystic Dysplastic Kidney Disease: An In-Utero Diagnosis.多囊性发育不良肾病:宫内诊断
Cureus. 2023 Apr 18;15(4):e37786. doi: 10.7759/cureus.37786. eCollection 2023 Apr.
2
A clinical predictive model of renal injury in children with congenital solitary functioning kidney.儿童先天性孤立功能肾损伤的临床预测模型。
Pediatr Nephrol. 2019 Mar;34(3):465-474. doi: 10.1007/s00467-018-4111-3. Epub 2018 Oct 15.
3
Large Multicystic Dysplastic Kidney Mimicking a Large Cystic Renal Neoplasm.酷似大囊性肾肿瘤的巨大多囊性发育不良肾
J Clin Diagn Res. 2017 May;11(5):PD03-PD04. doi: 10.7860/JCDR/2017/24226.9887. Epub 2017 May 1.
4
Unilateral multicystic dysplastic kidney: single-center experience.单侧多囊性发育不良肾:单中心经验
Pediatr Nephrol. 2009 Jan;24(1):99-104. doi: 10.1007/s00467-008-0942-7. Epub 2008 Aug 12.
5
Management and etiology of the unilateral multicystic dysplastic kidney: a review.单侧多囊性发育不良肾的管理与病因学:综述
Pediatr Nephrol. 2009 Feb;24(2):233-41. doi: 10.1007/s00467-008-0828-8. Epub 2008 May 15.