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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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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. |
format | Online Article Text |
id | pubmed-7393695 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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