儿童年龄组的多发性肾脏发育异常疾病：5例系列病例

IF 0.1 Q4 MEDICINE, GENERAL & INTERNAL

Journal of the Scientific Society Pub Date : 2023-01-01 DOI:10.4103/jss.jss_137_22

Sibnath Gayen, A. Chowdhury, Picaso Chowdhury, P. Halder, Damini Dutta, P. Chakraborty

{"title":"儿童年龄组的多发性肾脏发育异常疾病：5例系列病例","authors":"Sibnath Gayen, A. Chowdhury, Picaso Chowdhury, P. Halder, Damini Dutta, P. Chakraborty","doi":"10.4103/jss.jss_137_22","DOIUrl":null,"url":null,"abstract":"Multicystic dysplastic kidney (MCDK) is a congenital somatic maldevelopment in which the renal cortex is replaced by numerous cysts of varying sizes with insinuating dysplastic parenchyma in between. In 76% of cases, it is unilateral occurring on the left kidney. The condition could be diagnosed by ultrasound during pregnancy or after delivery. According to various studies, it follows a benign course and can be managed conservatively. Here, we present a series of five cases of unilateral MCDK that required surgical management due to either parent's psychosocial constraints or incidental discovery during surgery.","PeriodicalId":55681,"journal":{"name":"Journal of the Scientific Society","volume":null,"pages":null},"PeriodicalIF":0.1000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Multicystic dysplastic disease of kidney in pediatric age group: A series of five cases\",\"authors\":\"Sibnath Gayen, A. Chowdhury, Picaso Chowdhury, P. Halder, Damini Dutta, P. Chakraborty\",\"doi\":\"10.4103/jss.jss_137_22\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Multicystic dysplastic kidney (MCDK) is a congenital somatic maldevelopment in which the renal cortex is replaced by numerous cysts of varying sizes with insinuating dysplastic parenchyma in between. In 76% of cases, it is unilateral occurring on the left kidney. The condition could be diagnosed by ultrasound during pregnancy or after delivery. According to various studies, it follows a benign course and can be managed conservatively. Here, we present a series of five cases of unilateral MCDK that required surgical management due to either parent's psychosocial constraints or incidental discovery during surgery.\",\"PeriodicalId\":55681,\"journal\":{\"name\":\"Journal of the Scientific Society\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.1000,\"publicationDate\":\"2023-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of the Scientific Society\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.4103/jss.jss_137_22\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"MEDICINE, GENERAL & INTERNAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of the Scientific Society","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4103/jss.jss_137_22","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}

引用次数: 0

摘要

多囊性发育不良肾脏（MCDK）是一种先天性体细胞发育不良，肾皮质被大量大小不等的囊肿所取代，其间隐含着发育不良的实质。76%的病例单侧发生在左肾。这种情况可以在怀孕期间或产后通过超声波进行诊断。根据各种研究，它遵循良性过程，可以保守治疗。在这里，我们介绍了一系列五例单侧MCDK病例，由于父母的心理社会限制或手术中的偶然发现，这些病例需要手术治疗。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

查看原文本刊更多论文

Multicystic dysplastic disease of kidney in pediatric age group: A series of five cases

Multicystic dysplastic kidney (MCDK) is a congenital somatic maldevelopment in which the renal cortex is replaced by numerous cysts of varying sizes with insinuating dysplastic parenchyma in between. In 76% of cases, it is unilateral occurring on the left kidney. The condition could be diagnosed by ultrasound during pregnancy or after delivery. According to various studies, it follows a benign course and can be managed conservatively. Here, we present a series of five cases of unilateral MCDK that required surgical management due to either parent's psychosocial constraints or incidental discovery during surgery.

求助全文

通过发布文献求助，成功后即可免费获取论文全文。去求助

来源期刊

Journal of the Scientific Society MEDICINE, GENERAL & INTERNAL-

自引率

33.30%

发文量

审稿时长

36 weeks