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Large para-testicular intra-scrotal malignant peripheral nerve sheath tumor managed with radical penectomy: A case report

Neurofibromatosis 1 is a relatively rare genetic disease characterized by widespread neurofibromas originating from the peripheral nervous system. Most growths are benign, but some carry a risk of transformation to malignant peripheral nerve sheath tumors. Although these growths can be found anywher...

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Detalles Bibliográficos
Autores principales: Kazarian, Austin G., West, Jeremy M., Brown, James A., Erickson, Bradley A., Gellhaus, Paul T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8102162/
https://www.ncbi.nlm.nih.gov/pubmed/33996500
http://dx.doi.org/10.1016/j.eucr.2021.101695
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author Kazarian, Austin G.
West, Jeremy M.
Brown, James A.
Erickson, Bradley A.
Gellhaus, Paul T.
author_facet Kazarian, Austin G.
West, Jeremy M.
Brown, James A.
Erickson, Bradley A.
Gellhaus, Paul T.
author_sort Kazarian, Austin G.
collection PubMed
description Neurofibromatosis 1 is a relatively rare genetic disease characterized by widespread neurofibromas originating from the peripheral nervous system. Most growths are benign, but some carry a risk of transformation to malignant peripheral nerve sheath tumors. Although these growths can be found anywhere in the body, they are rarely found in the male external genitalia. This report discusses a case of a 25-year-old male patient with neurofibromatosis 1 presenting with a scrotal mass found to have a very large para-testicular intra-scrotal malignant peripheral nerve sheath tumor that required testicle-sparing radical penectomy.
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spelling pubmed-81021622021-05-14 Large para-testicular intra-scrotal malignant peripheral nerve sheath tumor managed with radical penectomy: A case report Kazarian, Austin G. West, Jeremy M. Brown, James A. Erickson, Bradley A. Gellhaus, Paul T. Urol Case Rep Oncology Neurofibromatosis 1 is a relatively rare genetic disease characterized by widespread neurofibromas originating from the peripheral nervous system. Most growths are benign, but some carry a risk of transformation to malignant peripheral nerve sheath tumors. Although these growths can be found anywhere in the body, they are rarely found in the male external genitalia. This report discusses a case of a 25-year-old male patient with neurofibromatosis 1 presenting with a scrotal mass found to have a very large para-testicular intra-scrotal malignant peripheral nerve sheath tumor that required testicle-sparing radical penectomy. Elsevier 2021-04-26 /pmc/articles/PMC8102162/ /pubmed/33996500 http://dx.doi.org/10.1016/j.eucr.2021.101695 Text en Published by Elsevier Inc. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Oncology
Kazarian, Austin G.
West, Jeremy M.
Brown, James A.
Erickson, Bradley A.
Gellhaus, Paul T.
Large para-testicular intra-scrotal malignant peripheral nerve sheath tumor managed with radical penectomy: A case report
title Large para-testicular intra-scrotal malignant peripheral nerve sheath tumor managed with radical penectomy: A case report
title_full Large para-testicular intra-scrotal malignant peripheral nerve sheath tumor managed with radical penectomy: A case report
title_fullStr Large para-testicular intra-scrotal malignant peripheral nerve sheath tumor managed with radical penectomy: A case report
title_full_unstemmed Large para-testicular intra-scrotal malignant peripheral nerve sheath tumor managed with radical penectomy: A case report
title_short Large para-testicular intra-scrotal malignant peripheral nerve sheath tumor managed with radical penectomy: A case report
title_sort large para-testicular intra-scrotal malignant peripheral nerve sheath tumor managed with radical penectomy: a case report
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8102162/
https://www.ncbi.nlm.nih.gov/pubmed/33996500
http://dx.doi.org/10.1016/j.eucr.2021.101695
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