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A Unique Case of Intraabdominal Polyorchidism: A Case Study
Background. Polyorchidism, alternatively supernumerary testes (SNT), is a condition where an individual is born with more than two testicles. This congenital anomaly is quite rare and the literature has described various presentations. Questions/Purposes. To our knowledge, this presentation of polyo...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5045993/ https://www.ncbi.nlm.nih.gov/pubmed/27722006 http://dx.doi.org/10.1155/2016/2729614 |
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author | Otero, Javier Ben-Yakar, Natalie Alemayehu, Biruk Kozusko, Steven D. Borao, Frank Vates III, Thomas S. |
author_facet | Otero, Javier Ben-Yakar, Natalie Alemayehu, Biruk Kozusko, Steven D. Borao, Frank Vates III, Thomas S. |
author_sort | Otero, Javier |
collection | PubMed |
description | Background. Polyorchidism, alternatively supernumerary testes (SNT), is a condition where an individual is born with more than two testicles. This congenital anomaly is quite rare and the literature has described various presentations. Questions/Purposes. To our knowledge, this presentation of polyorchidism has yet to be described in the literature. The goal of this case study is to add to the pediatric, general, and urologic surgery's body of knowledge of the subject matter. Case Study. A nine-month-old boy was admitted for an impalpable right testis and phimosis. At the time of surgical exploration, there appeared to be polyorchid testis on the right-hand side, with three masses that potentially appeared to be undescended testes. Discussion. Proponents of a conservative approach argue that infertility is common in patients with polyorchidism and, by preserving a potentially functional SNT, there may be improved spermatogenesis. When performing definitive surgical treatment, meticulous intra-abdominal and intrainguinal exploration must be undertaken. Orchiopexy should be performed to reduce the chances of torsion, malignancy, and infertility. Conclusion. Our case is important to the literature as it is the first known case of polyorchidism with 3 SNT on the right side, located intra-abdominally, and in a patient less than 1 year of age. |
format | Online Article Text |
id | pubmed-5045993 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-50459932016-10-09 A Unique Case of Intraabdominal Polyorchidism: A Case Study Otero, Javier Ben-Yakar, Natalie Alemayehu, Biruk Kozusko, Steven D. Borao, Frank Vates III, Thomas S. Case Rep Urol Case Report Background. Polyorchidism, alternatively supernumerary testes (SNT), is a condition where an individual is born with more than two testicles. This congenital anomaly is quite rare and the literature has described various presentations. Questions/Purposes. To our knowledge, this presentation of polyorchidism has yet to be described in the literature. The goal of this case study is to add to the pediatric, general, and urologic surgery's body of knowledge of the subject matter. Case Study. A nine-month-old boy was admitted for an impalpable right testis and phimosis. At the time of surgical exploration, there appeared to be polyorchid testis on the right-hand side, with three masses that potentially appeared to be undescended testes. Discussion. Proponents of a conservative approach argue that infertility is common in patients with polyorchidism and, by preserving a potentially functional SNT, there may be improved spermatogenesis. When performing definitive surgical treatment, meticulous intra-abdominal and intrainguinal exploration must be undertaken. Orchiopexy should be performed to reduce the chances of torsion, malignancy, and infertility. Conclusion. Our case is important to the literature as it is the first known case of polyorchidism with 3 SNT on the right side, located intra-abdominally, and in a patient less than 1 year of age. Hindawi Publishing Corporation 2016 2016-07-13 /pmc/articles/PMC5045993/ /pubmed/27722006 http://dx.doi.org/10.1155/2016/2729614 Text en Copyright © 2016 Javier Otero et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Otero, Javier Ben-Yakar, Natalie Alemayehu, Biruk Kozusko, Steven D. Borao, Frank Vates III, Thomas S. A Unique Case of Intraabdominal Polyorchidism: A Case Study |
title | A Unique Case of Intraabdominal Polyorchidism: A Case Study |
title_full | A Unique Case of Intraabdominal Polyorchidism: A Case Study |
title_fullStr | A Unique Case of Intraabdominal Polyorchidism: A Case Study |
title_full_unstemmed | A Unique Case of Intraabdominal Polyorchidism: A Case Study |
title_short | A Unique Case of Intraabdominal Polyorchidism: A Case Study |
title_sort | unique case of intraabdominal polyorchidism: a case study |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5045993/ https://www.ncbi.nlm.nih.gov/pubmed/27722006 http://dx.doi.org/10.1155/2016/2729614 |
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