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Transverse testicular ectopia with Müllerian duct remnant in an incarcerated congenital inguinal hernia – a case report

BACKGROUND: Transverse testicular ectopia (TTE) is a rare anomaly characterized by both testes descending through a single inguinal canal. In this report, the diagnosis of TTE was discovered in the event of an incarcerated congenital inguinal hernia in a neonate. CASE PRESENTATION: We present a case...

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Autores principales: Kotb, Mostafa, Hassan, Ahmed, Abouheba, Mohamed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7393695/
https://www.ncbi.nlm.nih.gov/pubmed/32731851
http://dx.doi.org/10.1186/s12894-020-00680-9
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author Kotb, Mostafa
Hassan, Ahmed
Abouheba, Mohamed
author_facet Kotb, Mostafa
Hassan, Ahmed
Abouheba, Mohamed
author_sort Kotb, Mostafa
collection PubMed
description BACKGROUND: Transverse testicular ectopia (TTE) is a rare anomaly characterized by both testes descending through a single inguinal canal. In this report, the diagnosis of TTE was discovered in the event of an incarcerated congenital inguinal hernia in a neonate. CASE PRESENTATION: We present a case of TTE accompanied by persistent Müllerian duct structures (PMDS) that had been discovered incidentally during inguinal exploration of a 26-day-old boy who presented with an incarcerated congenital inguinal hernia on the right side and left cryptochidism on the left side. The pathogenesis, approach and proposed management of TTE are discussed. CONCLUSION: TTE is an extremely rare anomaly, especially in neonates, and should be suspected in patients presenting with inguinal hernia on one side and cryptorchidism on the other side.
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spelling pubmed-73936952020-08-04 Transverse testicular ectopia with Müllerian duct remnant in an incarcerated congenital inguinal hernia – a case report Kotb, Mostafa Hassan, Ahmed Abouheba, Mohamed BMC Urol Case Report BACKGROUND: Transverse testicular ectopia (TTE) is a rare anomaly characterized by both testes descending through a single inguinal canal. In this report, the diagnosis of TTE was discovered in the event of an incarcerated congenital inguinal hernia in a neonate. CASE PRESENTATION: We present a case of TTE accompanied by persistent Müllerian duct structures (PMDS) that had been discovered incidentally during inguinal exploration of a 26-day-old boy who presented with an incarcerated congenital inguinal hernia on the right side and left cryptochidism on the left side. The pathogenesis, approach and proposed management of TTE are discussed. CONCLUSION: TTE is an extremely rare anomaly, especially in neonates, and should be suspected in patients presenting with inguinal hernia on one side and cryptorchidism on the other side. BioMed Central 2020-07-30 /pmc/articles/PMC7393695/ /pubmed/32731851 http://dx.doi.org/10.1186/s12894-020-00680-9 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Case Report
Kotb, Mostafa
Hassan, Ahmed
Abouheba, Mohamed
Transverse testicular ectopia with Müllerian duct remnant in an incarcerated congenital inguinal hernia – a case report
title Transverse testicular ectopia with Müllerian duct remnant in an incarcerated congenital inguinal hernia – a case report
title_full Transverse testicular ectopia with Müllerian duct remnant in an incarcerated congenital inguinal hernia – a case report
title_fullStr Transverse testicular ectopia with Müllerian duct remnant in an incarcerated congenital inguinal hernia – a case report
title_full_unstemmed Transverse testicular ectopia with Müllerian duct remnant in an incarcerated congenital inguinal hernia – a case report
title_short Transverse testicular ectopia with Müllerian duct remnant in an incarcerated congenital inguinal hernia – a case report
title_sort transverse testicular ectopia with müllerian duct remnant in an incarcerated congenital inguinal hernia – a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7393695/
https://www.ncbi.nlm.nih.gov/pubmed/32731851
http://dx.doi.org/10.1186/s12894-020-00680-9
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AT abouhebamohamed transversetesticularectopiawithmullerianductremnantinanincarceratedcongenitalinguinalherniaacasereport