Bladder Exstrophy in a Female Fetus: Ultrasound and Autopsy Findings.

IF 0.8 4区 医学 Q4 PATHOLOGY
Fetal and Pediatric Pathology Pub Date : 2026-03-01 Epub Date: 2026-03-04 DOI:10.1080/15513815.2026.2628770
Maria Paola Bonasoni, Giuseppina Comitini, Andrea Musarò, Flavio Vanacore, Immacolata Blasi, Giovanna Botticelli, Veronica Barbieri, Maria Marinelli, Francesca Peluso, Livia Garavelli, Khush Shah, Lorenzo Aguzzoli, Mariangela Pati
{"title":"Bladder Exstrophy in a Female Fetus: Ultrasound and Autopsy Findings.","authors":"Maria Paola Bonasoni, Giuseppina Comitini, Andrea Musarò, Flavio Vanacore, Immacolata Blasi, Giovanna Botticelli, Veronica Barbieri, Maria Marinelli, Francesca Peluso, Livia Garavelli, Khush Shah, Lorenzo Aguzzoli, Mariangela Pati","doi":"10.1080/15513815.2026.2628770","DOIUrl":null,"url":null,"abstract":"<p><p><b>Introduction:</b> Bladder exstrophy (BE) is a congenital anomaly within the exstrophy-epispadias complex (EEC), characterized by a defect in the closure of the lower abdominal wall and bladder. <b>Case report:</b> A female fetus at 20 weeks + 2 days showed at ultrasound (US) a homogeneous echogenic mass with a lobulated surface, protruding from the anterior lower abdominal wall. The bladder was not visualized. Doppler US displayed umbilical arteries laterally to the mass. The kidneys appeared normal. Amniotic fluid was regular. Legal termination of pregnancy occurred at 21 weeks + 4 days. Autopsy grossly and histologically confirmed BE. Microscopically, BE was layered by an urothelial-like epithelial layer and underneath, the muscularis propria was disarrayed with scarce nerve fibers, evidenced by immunohistochemistry for S-100. <b>Conclusion:</b> In case of prenatal diagnosis of BE, multidisciplinary counseling is mandatory for appropriate clinical management.</p>","PeriodicalId":50452,"journal":{"name":"Fetal and Pediatric Pathology","volume":" ","pages":"132-142"},"PeriodicalIF":0.8000,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Fetal and Pediatric Pathology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1080/15513815.2026.2628770","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/3/4 0:00:00","PubModel":"Epub","JCR":"Q4","JCRName":"PATHOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Introduction: Bladder exstrophy (BE) is a congenital anomaly within the exstrophy-epispadias complex (EEC), characterized by a defect in the closure of the lower abdominal wall and bladder. Case report: A female fetus at 20 weeks + 2 days showed at ultrasound (US) a homogeneous echogenic mass with a lobulated surface, protruding from the anterior lower abdominal wall. The bladder was not visualized. Doppler US displayed umbilical arteries laterally to the mass. The kidneys appeared normal. Amniotic fluid was regular. Legal termination of pregnancy occurred at 21 weeks + 4 days. Autopsy grossly and histologically confirmed BE. Microscopically, BE was layered by an urothelial-like epithelial layer and underneath, the muscularis propria was disarrayed with scarce nerve fibers, evidenced by immunohistochemistry for S-100. Conclusion: In case of prenatal diagnosis of BE, multidisciplinary counseling is mandatory for appropriate clinical management.

女性胎儿膀胱外翻:超声和尸检结果。
简介:膀胱外翻(BE)是外翻-上膈复合体(EEC)内的一种先天性异常,其特征是下腹壁和膀胱的闭合缺陷。病例报告:一个20周+ 2天的女胎儿在超声检查(US)显示一个均匀的回声肿块,表面呈分叶状,从前下腹壁突出。膀胱未见。多普勒超声显示肿块外侧的脐动脉。肾脏显示正常。羊水正常。法定终止妊娠发生在21周+ 4天。尸检大体和组织学证实为BE。显微镜下,BE呈尿路上皮样上皮层状,S-100免疫组化证实其固有肌层紊乱,神经纤维稀少。结论:在产前诊断为BE的情况下,多学科咨询对临床管理是必要的。
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
CiteScore
3.00
自引率
0.00%
发文量
68
审稿时长
6-12 weeks
期刊介绍: Fetal and Pediatric Pathology is an established bimonthly international journal that publishes data on diseases of the developing embryo, newborns, children, and adolescents. The journal publishes original and review articles and reportable case reports. The expanded scope of the journal encompasses molecular basis of genetic disorders; molecular basis of diseases that lead to implantation failures; molecular basis of abnormal placentation; placentology and molecular basis of habitual abortion; intrauterine development and molecular basis of embryonic death; pathogenisis and etiologic factors involved in sudden infant death syndrome; the underlying molecular basis, and pathogenesis of diseases that lead to morbidity and mortality in newborns; prenatal, perinatal, and pediatric diseases and molecular basis of diseases of childhood including solid tumors and tumors of the hematopoietic system; and experimental and molecular pathology.
×
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
小红书