Kidney Agenesis and Müllerian Duct Anomalies: A Report of Two Cases and Literature Review.

Q3 Medicine
Acta Medica Lituanica Pub Date : 2025-01-01 Epub Date: 2025-02-18 DOI:10.15388/Amed.2025.32.1.7
Kamilė Donielaitė-Anisė, Rytis Marozas, Žana Bumbulienė, Augustina Jankauskienė
{"title":"Kidney Agenesis and Müllerian Duct Anomalies: A Report of Two Cases and Literature Review.","authors":"Kamilė Donielaitė-Anisė, Rytis Marozas, Žana Bumbulienė, Augustina Jankauskienė","doi":"10.15388/Amed.2025.32.1.7","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>The association between urinary tract anomalies and <i>Müllerian duct anomalies</i> (MDA) is well-known, due to their shared embryonic origin. Disruptions in early development can significantly affect both the kidney and reproductive systems. This article presents two cases illustrating the coexistence of kidney agenesis and MDA in girls, followed by a literature review.</p><p><strong>Materials and methods: </strong>A literature search was conducted on <i>PubMed</i>, focusing on publications from 2000 to 2024 by using keywords: 'kidney agenesis', 'renal agenesis', 'Müllerian duct anomalies', 'OHVIRA' (obstructed hemivagina and ipsilateral renal anomaly), and 'Herlyn-Werner-Wunderlich syndrome'. The PRISMA guidelines were followed for the study selection. Additionally, two cases managed at Vilnius University Hospital Santaros Klinikos between 2022 and 2024 are presented.</p><p><strong>Results: </strong>The literature search yielded 32 articles encompassing data on 43 girls with an average age of 11.8 years. In 54% of the cases, the diagnosis of kidney agenesis was concurrent with identifying MDA. In other cases, kidney anomalies were detected earlier, including 6 cases identified prenatally. Type III MDA, as classified by the <i>American Fertility Society</i>, was the most common variety. Premenarche diagnosis of MDA was made in 11.9% of the cases. In more than half of the cases, MDA was identified due to complaints necessitating consultations, mostly leading to urgent surgical interventions. At our hospital, a 9-year-old and a 14-year-old were diagnosed with Herlyn-Werner-Wunderlich syndrome. Kidney agenesis was diagnosed prior to MDA in both cases. For the 9-year-old girl, MDA was found incidentally on ultrasound, while the other required consultation and an urgent surgery due to symptoms.</p><p><strong>Conclusions: </strong>Unilateral kidney agenesis frequently co-occurs with Müllerian duct anomalies, highlighting the need for comprehensive evaluations in affected patients. An early diagnosis and management of MDA are crucial to prevent complications. An increased clinical awareness and further research are necessary to enhance early detection and patient outcomes.</p>","PeriodicalId":34365,"journal":{"name":"Acta Medica Lituanica","volume":"32 1","pages":"229-235"},"PeriodicalIF":0.0000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12239172/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Acta Medica Lituanica","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.15388/Amed.2025.32.1.7","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/2/18 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

Abstract

Background: The association between urinary tract anomalies and Müllerian duct anomalies (MDA) is well-known, due to their shared embryonic origin. Disruptions in early development can significantly affect both the kidney and reproductive systems. This article presents two cases illustrating the coexistence of kidney agenesis and MDA in girls, followed by a literature review.

Materials and methods: A literature search was conducted on PubMed, focusing on publications from 2000 to 2024 by using keywords: 'kidney agenesis', 'renal agenesis', 'Müllerian duct anomalies', 'OHVIRA' (obstructed hemivagina and ipsilateral renal anomaly), and 'Herlyn-Werner-Wunderlich syndrome'. The PRISMA guidelines were followed for the study selection. Additionally, two cases managed at Vilnius University Hospital Santaros Klinikos between 2022 and 2024 are presented.

Results: The literature search yielded 32 articles encompassing data on 43 girls with an average age of 11.8 years. In 54% of the cases, the diagnosis of kidney agenesis was concurrent with identifying MDA. In other cases, kidney anomalies were detected earlier, including 6 cases identified prenatally. Type III MDA, as classified by the American Fertility Society, was the most common variety. Premenarche diagnosis of MDA was made in 11.9% of the cases. In more than half of the cases, MDA was identified due to complaints necessitating consultations, mostly leading to urgent surgical interventions. At our hospital, a 9-year-old and a 14-year-old were diagnosed with Herlyn-Werner-Wunderlich syndrome. Kidney agenesis was diagnosed prior to MDA in both cases. For the 9-year-old girl, MDA was found incidentally on ultrasound, while the other required consultation and an urgent surgery due to symptoms.

Conclusions: Unilateral kidney agenesis frequently co-occurs with Müllerian duct anomalies, highlighting the need for comprehensive evaluations in affected patients. An early diagnosis and management of MDA are crucial to prevent complications. An increased clinical awareness and further research are necessary to enhance early detection and patient outcomes.

肾发育不全及胆管异常2例报告并文献复习。
背景:泌尿道异常和勒氏管异常(MDA)之间的关系是众所周知的,因为它们有共同的胚胎起源。早期发育的中断会严重影响肾脏和生殖系统。本文提出了两个例子说明共存肾发育不全和丙二醛在女孩,其次是文献综述。材料与方法:在PubMed检索文献,检索2000 - 2024年发表的文献,检索关键词:“肾发育不全”、“肾发育不全”、“勒氏管异常”、“OHVIRA”(半阴道梗阻及同侧肾异常)、“herlin - werner - wunderlich综合征”。研究选择遵循PRISMA指南。此外,还介绍了维尔纽斯大学Santaros Klinikos医院在2022年至2024年期间管理的两个病例。结果:文献检索得到32篇文章,包含43名平均年龄11.8岁的女孩的数据。在54%的病例中,肾脏发育不全的诊断与MDA的检测同时进行。在其他病例中,肾脏异常发现较早,包括6例产前发现。根据美国生育学会的分类,III型MDA是最常见的品种。11.9%的病例在产前诊断为MDA。在一半以上的病例中,由于需要咨询的投诉而确定了MDA,大多数导致紧急手术干预。在我们医院,一个9岁的孩子和一个14岁的孩子被诊断为herlin - werner - wunderlich综合征。两例患者均在MDA检测前诊断为肾脏发育不全。对于9岁的女孩,MDA是在超声波中偶然发现的,而另一个则因症状需要咨询和紧急手术。结论:单侧肾脏发育不全经常与腰外侧胆管异常同时发生,强调了对患者进行综合评估的必要性。早期诊断和管理MDA是预防并发症的关键。提高临床意识和进一步研究是提高早期发现和患者预后的必要条件。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Acta Medica Lituanica
Acta Medica Lituanica Medicine-General Medicine
CiteScore
0.70
自引率
0.00%
发文量
33
审稿时长
16 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信