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Transverse testicular ectopia, a case report and review of literature

Crossed testicular ectopia (CTE)/transverse testicular ectopia (TTE) is a rare but well known congenital anomaly, in which both gonads migrate toward the same hemiscrotum. It is usually associated with other abnormalities such as persistent Mullerian duct syndrome, true hermaphroditism, inguinal her...

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Autores principales: Moslemi, Mohammad Kazem, Ebadzadeh, Mohammad Reza, Al-Mousawi, Shabir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: German Medical Science GMS Publishing House 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3141845/
https://www.ncbi.nlm.nih.gov/pubmed/21808600
http://dx.doi.org/10.3205/000138
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author Moslemi, Mohammad Kazem
Ebadzadeh, Mohammad Reza
Al-Mousawi, Shabir
author_facet Moslemi, Mohammad Kazem
Ebadzadeh, Mohammad Reza
Al-Mousawi, Shabir
author_sort Moslemi, Mohammad Kazem
collection PubMed
description Crossed testicular ectopia (CTE)/transverse testicular ectopia (TTE) is a rare but well known congenital anomaly, in which both gonads migrate toward the same hemiscrotum. It is usually associated with other abnormalities such as persistent Mullerian duct syndrome, true hermaphroditism, inguinal hernia, hypospadias, pseudohermaphroditism, and scrotal anomalies. About 100 cases of transverse testicular ectopia have been reported in published studies. We report a case of transverse testicular ectopia in an 8-month-old boy who presented with right inguinal hernia and nonpalpable left testis. On exploration, both testes were present in the right inguinal region. Bilateral orchiopexy was performed by crossing the left testis in the extra-peritoneal space and ipsilateral scrotal orchiopexy. The diagnosis could not be made preoperatively in most of reported cases.
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spelling pubmed-31418452011-08-01 Transverse testicular ectopia, a case report and review of literature Moslemi, Mohammad Kazem Ebadzadeh, Mohammad Reza Al-Mousawi, Shabir Ger Med Sci Article Crossed testicular ectopia (CTE)/transverse testicular ectopia (TTE) is a rare but well known congenital anomaly, in which both gonads migrate toward the same hemiscrotum. It is usually associated with other abnormalities such as persistent Mullerian duct syndrome, true hermaphroditism, inguinal hernia, hypospadias, pseudohermaphroditism, and scrotal anomalies. About 100 cases of transverse testicular ectopia have been reported in published studies. We report a case of transverse testicular ectopia in an 8-month-old boy who presented with right inguinal hernia and nonpalpable left testis. On exploration, both testes were present in the right inguinal region. Bilateral orchiopexy was performed by crossing the left testis in the extra-peritoneal space and ipsilateral scrotal orchiopexy. The diagnosis could not be made preoperatively in most of reported cases. German Medical Science GMS Publishing House 2011-07-07 /pmc/articles/PMC3141845/ /pubmed/21808600 http://dx.doi.org/10.3205/000138 Text en Copyright © 2011 Moslemi et al. http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc-nd/3.0/deed.en). You are free to copy, distribute and transmit the work, provided the original author and source are credited.
spellingShingle Article
Moslemi, Mohammad Kazem
Ebadzadeh, Mohammad Reza
Al-Mousawi, Shabir
Transverse testicular ectopia, a case report and review of literature
title Transverse testicular ectopia, a case report and review of literature
title_full Transverse testicular ectopia, a case report and review of literature
title_fullStr Transverse testicular ectopia, a case report and review of literature
title_full_unstemmed Transverse testicular ectopia, a case report and review of literature
title_short Transverse testicular ectopia, a case report and review of literature
title_sort transverse testicular ectopia, a case report and review of literature
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3141845/
https://www.ncbi.nlm.nih.gov/pubmed/21808600
http://dx.doi.org/10.3205/000138
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