Herlyn-Werner-Wünderlich综合征:一系列病例

IF 0.1 Q4 OBSTETRICS & GYNECOLOGY
M. Castillo Lara, L. De Pablo Zamora, E. Pozuelo Solis
{"title":"Herlyn-Werner-Wünderlich综合征:一系列病例","authors":"M. Castillo Lara,&nbsp;L. De Pablo Zamora,&nbsp;E. Pozuelo Solis","doi":"10.1016/j.gine.2023.100912","DOIUrl":null,"url":null,"abstract":"<div><h3>Introduction</h3><p>Herlyn–Werner–Wünderlich syndrome is a uterine malformation characterized by uterus didelphys, obstructed hemivagina and ipsilateral renal agenesis.</p></div><div><h3>Clinical findings</h3><p>The manifestation of the disease is widely diverse; it is usually diagnosed after menarche, with dysmenorrhea and abnormal uterine bleeding; it is also associated with infertility.</p></div><div><h3>Main diagnosis</h3><p>Four clinical cases, their diagnosis are reported here.</p></div><div><h3>Therapeutic interventions and results</h3><p>The treatment and results of these four patients are described here.</p></div><div><h3>Conclusion</h3><p>When studying uterine malformation it is important to consider this rare disease to avoid possible complications and giving the patient a correct diagnose and treatment. The hysteroscopy resection of the longitudinal vaginal septum in those symptomatic patients with hematocolpos should be considered as a good option for treatment.</p></div>","PeriodicalId":41294,"journal":{"name":"Clinica e Investigacion en Ginecologia y Obstetricia","volume":"51 1","pages":"Article 100912"},"PeriodicalIF":0.1000,"publicationDate":"2023-09-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Herlyn–Werner–Wünderlich syndrome: A case series\",\"authors\":\"M. Castillo Lara,&nbsp;L. De Pablo Zamora,&nbsp;E. Pozuelo Solis\",\"doi\":\"10.1016/j.gine.2023.100912\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Introduction</h3><p>Herlyn–Werner–Wünderlich syndrome is a uterine malformation characterized by uterus didelphys, obstructed hemivagina and ipsilateral renal agenesis.</p></div><div><h3>Clinical findings</h3><p>The manifestation of the disease is widely diverse; it is usually diagnosed after menarche, with dysmenorrhea and abnormal uterine bleeding; it is also associated with infertility.</p></div><div><h3>Main diagnosis</h3><p>Four clinical cases, their diagnosis are reported here.</p></div><div><h3>Therapeutic interventions and results</h3><p>The treatment and results of these four patients are described here.</p></div><div><h3>Conclusion</h3><p>When studying uterine malformation it is important to consider this rare disease to avoid possible complications and giving the patient a correct diagnose and treatment. The hysteroscopy resection of the longitudinal vaginal septum in those symptomatic patients with hematocolpos should be considered as a good option for treatment.</p></div>\",\"PeriodicalId\":41294,\"journal\":{\"name\":\"Clinica e Investigacion en Ginecologia y Obstetricia\",\"volume\":\"51 1\",\"pages\":\"Article 100912\"},\"PeriodicalIF\":0.1000,\"publicationDate\":\"2023-09-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Clinica e Investigacion en Ginecologia y Obstetricia\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0210573X23000825\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"OBSTETRICS & GYNECOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinica e Investigacion en Ginecologia y Obstetricia","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0210573X23000825","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"OBSTETRICS & GYNECOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

引言Herlyn–Werner–Wünderlich综合征是一种子宫畸形,其特征是子宫双胎、半阴道阻塞和同侧肾发育不全。临床发现本病表现广泛多样;通常在月经初潮后诊断,伴有痛经和异常子宫出血;它也与不孕有关。主要诊断本文报告4例临床病例及其诊断。治疗干预和结果本文介绍了这四名患者的治疗和结果。结论在研究子宫畸形时,重要的是要考虑这种罕见的疾病,以避免可能的并发症,并给予患者正确的诊断和治疗。对于有症状的阴道积血患者,宫腔镜下阴道纵隔切除术应被视为一种良好的治疗选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Herlyn–Werner–Wünderlich syndrome: A case series

Introduction

Herlyn–Werner–Wünderlich syndrome is a uterine malformation characterized by uterus didelphys, obstructed hemivagina and ipsilateral renal agenesis.

Clinical findings

The manifestation of the disease is widely diverse; it is usually diagnosed after menarche, with dysmenorrhea and abnormal uterine bleeding; it is also associated with infertility.

Main diagnosis

Four clinical cases, their diagnosis are reported here.

Therapeutic interventions and results

The treatment and results of these four patients are described here.

Conclusion

When studying uterine malformation it is important to consider this rare disease to avoid possible complications and giving the patient a correct diagnose and treatment. The hysteroscopy resection of the longitudinal vaginal septum in those symptomatic patients with hematocolpos should be considered as a good option for treatment.

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
CiteScore
0.20
自引率
0.00%
发文量
54
期刊介绍: Una excelente publicación para mantenerse al día en los temas de máximo interés de la ginecología de vanguardia. Resulta idónea tanto para el especialista en ginecología, como en obstetricia o en pediatría, y está presente en los más prestigiosos índices de referencia en medicina.
×
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:481959085
Book学术官方微信