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A rare case of paratesticular leiomyosarcoma
Paratesticular leiomyosarcoma is a rare tumour. It is seldom diagnosed pre-operatively and subsequent secondary resection is often required. Current treatment consensus comprises inguinal radical orchidectomy with high ligation of the spermatic cord. We present a case of a 74-year-old male with a 3-...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Oxford University Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6196989/ https://www.ncbi.nlm.nih.gov/pubmed/30364507 http://dx.doi.org/10.1093/jscr/rjy267 |
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author | Rezvani, Sean Bolton, James Crump, Ann |
author_facet | Rezvani, Sean Bolton, James Crump, Ann |
author_sort | Rezvani, Sean |
collection | PubMed |
description | Paratesticular leiomyosarcoma is a rare tumour. It is seldom diagnosed pre-operatively and subsequent secondary resection is often required. Current treatment consensus comprises inguinal radical orchidectomy with high ligation of the spermatic cord. We present a case of a 74-year-old male with a 3-year history of a painless right-sided scrotal mass which following excision was found to be an epididymal leiomyosarcoma. A review of literature and treatment is presented in this article. |
format | Online Article Text |
id | pubmed-6196989 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-61969892018-10-25 A rare case of paratesticular leiomyosarcoma Rezvani, Sean Bolton, James Crump, Ann J Surg Case Rep Case Report Paratesticular leiomyosarcoma is a rare tumour. It is seldom diagnosed pre-operatively and subsequent secondary resection is often required. Current treatment consensus comprises inguinal radical orchidectomy with high ligation of the spermatic cord. We present a case of a 74-year-old male with a 3-year history of a painless right-sided scrotal mass which following excision was found to be an epididymal leiomyosarcoma. A review of literature and treatment is presented in this article. Oxford University Press 2018-10-22 /pmc/articles/PMC6196989/ /pubmed/30364507 http://dx.doi.org/10.1093/jscr/rjy267 Text en Published by Oxford University Press and JSCR Publishing Ltd. All rights reserved. © The Author(s) 2018. 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 Rezvani, Sean Bolton, James Crump, Ann A rare case of paratesticular leiomyosarcoma |
title | A rare case of paratesticular leiomyosarcoma |
title_full | A rare case of paratesticular leiomyosarcoma |
title_fullStr | A rare case of paratesticular leiomyosarcoma |
title_full_unstemmed | A rare case of paratesticular leiomyosarcoma |
title_short | A rare case of paratesticular leiomyosarcoma |
title_sort | rare case of paratesticular leiomyosarcoma |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6196989/ https://www.ncbi.nlm.nih.gov/pubmed/30364507 http://dx.doi.org/10.1093/jscr/rjy267 |
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