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Triorchidism: A Rare Genitourinary Abnormality
Polyorchidism is an extremely rare congenital anomaly which refers to the presence of more than two testicles. There are very few reports of triorchidism in a 2 year old child. Polyorchidism is usually discovered incidentally. The most common anomalies associated with polyorchidism are inguinal hern...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2012
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3673357/ https://www.ncbi.nlm.nih.gov/pubmed/23741593 http://dx.doi.org/10.4103/2006-8808.110262 |
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author | Tonape, Trupti Singh, Gurjit Koushik, P. Tumepalli, Trinath |
author_facet | Tonape, Trupti Singh, Gurjit Koushik, P. Tumepalli, Trinath |
author_sort | Tonape, Trupti |
collection | PubMed |
description | Polyorchidism is an extremely rare congenital anomaly which refers to the presence of more than two testicles. There are very few reports of triorchidism in a 2 year old child. Polyorchidism is usually discovered incidentally. The most common anomalies associated with polyorchidism are inguinal hernia (30%), maldescended testis (15% to 30%), testicular torsion (13%) and hydrocele (9%). A 2-year-old child was brought with bilateral undescended testis with normal milestones. Ultrasonography of scrotum and abdomen showed both the testes to be in inguinal canal. Intra-operatively, on left side - there were two testes, which belonged to Leung III class and one testis on right side. Management of polyorchidism is still controversial. The management of polyorchidism will depend upon the location, size and anatomical organisation of the testicular drainage system and the age of the patient. |
format | Online Article Text |
id | pubmed-3673357 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-36733572013-06-05 Triorchidism: A Rare Genitourinary Abnormality Tonape, Trupti Singh, Gurjit Koushik, P. Tumepalli, Trinath J Surg Tech Case Rep Case Report Polyorchidism is an extremely rare congenital anomaly which refers to the presence of more than two testicles. There are very few reports of triorchidism in a 2 year old child. Polyorchidism is usually discovered incidentally. The most common anomalies associated with polyorchidism are inguinal hernia (30%), maldescended testis (15% to 30%), testicular torsion (13%) and hydrocele (9%). A 2-year-old child was brought with bilateral undescended testis with normal milestones. Ultrasonography of scrotum and abdomen showed both the testes to be in inguinal canal. Intra-operatively, on left side - there were two testes, which belonged to Leung III class and one testis on right side. Management of polyorchidism is still controversial. The management of polyorchidism will depend upon the location, size and anatomical organisation of the testicular drainage system and the age of the patient. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3673357/ /pubmed/23741593 http://dx.doi.org/10.4103/2006-8808.110262 Text en Copyright: © Journal of Surgical Technique and Case Report http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Tonape, Trupti Singh, Gurjit Koushik, P. Tumepalli, Trinath Triorchidism: A Rare Genitourinary Abnormality |
title | Triorchidism: A Rare Genitourinary Abnormality |
title_full | Triorchidism: A Rare Genitourinary Abnormality |
title_fullStr | Triorchidism: A Rare Genitourinary Abnormality |
title_full_unstemmed | Triorchidism: A Rare Genitourinary Abnormality |
title_short | Triorchidism: A Rare Genitourinary Abnormality |
title_sort | triorchidism: a rare genitourinary abnormality |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3673357/ https://www.ncbi.nlm.nih.gov/pubmed/23741593 http://dx.doi.org/10.4103/2006-8808.110262 |
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