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First reported case of paratesticular seminoma in a postpubertal cryptorchid testis

Cryptorchidism is a very common anomaly, affecting 2–4% of male infants and is more common in premature infants. The long-term outcome despite orchidopexy still remains problematic and controversial with a risk of developing cancer 5–10 times greater than normal. Paratesticular tumors are mostly ben...

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Autores principales: Elhajjar, Imad, Sayyid, Khalid, Mugharbil, Anas, Abtar, Houssam Khodor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5499890/
https://www.ncbi.nlm.nih.gov/pubmed/28698791
http://dx.doi.org/10.1093/jscr/rjx088
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author Elhajjar, Imad
Sayyid, Khalid
Mugharbil, Anas
Abtar, Houssam Khodor
author_facet Elhajjar, Imad
Sayyid, Khalid
Mugharbil, Anas
Abtar, Houssam Khodor
author_sort Elhajjar, Imad
collection PubMed
description Cryptorchidism is a very common anomaly, affecting 2–4% of male infants and is more common in premature infants. The long-term outcome despite orchidopexy still remains problematic and controversial with a risk of developing cancer 5–10 times greater than normal. Paratesticular tumors are mostly benign and very rare in children however malignant paratesticular tumors do arise, the most common being rhabdomyosarcoma. Primary paratesticular seminoma is extremely rare by itself and in most cases is associated with foci of seminoma within the testis. To the best of our knowledge, our case represents the fourth reported case of paratesticular seminoma in the published literature and being the first one in cryptorchid testis.
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spelling pubmed-54998902017-07-11 First reported case of paratesticular seminoma in a postpubertal cryptorchid testis Elhajjar, Imad Sayyid, Khalid Mugharbil, Anas Abtar, Houssam Khodor J Surg Case Rep Case Report Cryptorchidism is a very common anomaly, affecting 2–4% of male infants and is more common in premature infants. The long-term outcome despite orchidopexy still remains problematic and controversial with a risk of developing cancer 5–10 times greater than normal. Paratesticular tumors are mostly benign and very rare in children however malignant paratesticular tumors do arise, the most common being rhabdomyosarcoma. Primary paratesticular seminoma is extremely rare by itself and in most cases is associated with foci of seminoma within the testis. To the best of our knowledge, our case represents the fourth reported case of paratesticular seminoma in the published literature and being the first one in cryptorchid testis. Oxford University Press 2017-06-20 /pmc/articles/PMC5499890/ /pubmed/28698791 http://dx.doi.org/10.1093/jscr/rjx088 Text en Published by Oxford University Press and JSCR Publishing Ltd. All rights reserved. © The Author 2017. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Case Report
Elhajjar, Imad
Sayyid, Khalid
Mugharbil, Anas
Abtar, Houssam Khodor
First reported case of paratesticular seminoma in a postpubertal cryptorchid testis
title First reported case of paratesticular seminoma in a postpubertal cryptorchid testis
title_full First reported case of paratesticular seminoma in a postpubertal cryptorchid testis
title_fullStr First reported case of paratesticular seminoma in a postpubertal cryptorchid testis
title_full_unstemmed First reported case of paratesticular seminoma in a postpubertal cryptorchid testis
title_short First reported case of paratesticular seminoma in a postpubertal cryptorchid testis
title_sort first reported case of paratesticular seminoma in a postpubertal cryptorchid testis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5499890/
https://www.ncbi.nlm.nih.gov/pubmed/28698791
http://dx.doi.org/10.1093/jscr/rjx088
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