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Malignant Melanoma with Concurrent BRAF E586K and NRAS Q81K Mutations

Cutaneous melanoma is an aggressive malignant tumor of melanocytes which accounts for 80% of skin cancer-related deaths. A number of driver mutations have been identified in melanoma, with the mutually exclusive BRAF V600E and NRAS Q61A mutations together accounting for roughly 70% of mutations. Sim...

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Autores principales: Shackelford, Rodney, Pollen, Maressa, Vora, Moise, Jusion, Tamara T., Cotelingam, James, Nair, Binu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4035678/
https://www.ncbi.nlm.nih.gov/pubmed/24926260
http://dx.doi.org/10.1159/000362788
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author Shackelford, Rodney
Pollen, Maressa
Vora, Moise
Jusion, Tamara T.
Cotelingam, James
Nair, Binu
author_facet Shackelford, Rodney
Pollen, Maressa
Vora, Moise
Jusion, Tamara T.
Cotelingam, James
Nair, Binu
author_sort Shackelford, Rodney
collection PubMed
description Cutaneous melanoma is an aggressive malignant tumor of melanocytes which accounts for 80% of skin cancer-related deaths. A number of driver mutations have been identified in melanoma, with the mutually exclusive BRAF V600E and NRAS Q61A mutations together accounting for roughly 70% of mutations. Simultaneous BRAF V600E and NRAS Q61A mutations in melanoma are rare, with evidence suggesting that up to 2.9% (2/69) of primary cutaneous melanomas carry both mutations. Here we describe a 42-year-old man with concurrent BRAF E586K and NRAS Q81K driver mutations. To our knowledge, this is the first description of these driver mutations occurring simultaneously in primary cutaneous melanoma.
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spelling pubmed-40356782014-06-12 Malignant Melanoma with Concurrent BRAF E586K and NRAS Q81K Mutations Shackelford, Rodney Pollen, Maressa Vora, Moise Jusion, Tamara T. Cotelingam, James Nair, Binu Case Rep Oncol Published online: May, 2014 Cutaneous melanoma is an aggressive malignant tumor of melanocytes which accounts for 80% of skin cancer-related deaths. A number of driver mutations have been identified in melanoma, with the mutually exclusive BRAF V600E and NRAS Q61A mutations together accounting for roughly 70% of mutations. Simultaneous BRAF V600E and NRAS Q61A mutations in melanoma are rare, with evidence suggesting that up to 2.9% (2/69) of primary cutaneous melanomas carry both mutations. Here we describe a 42-year-old man with concurrent BRAF E586K and NRAS Q81K driver mutations. To our knowledge, this is the first description of these driver mutations occurring simultaneously in primary cutaneous melanoma. S. Karger AG 2014-05-08 /pmc/articles/PMC4035678/ /pubmed/24926260 http://dx.doi.org/10.1159/000362788 Text en Copyright © 2014 by S. Karger AG, Basel http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article licensed under the terms of the Creative Commons Attribution-NonCommercial 3.0 Unported license (CC BY-NC) (www.karger.com/OA-license), applicable to the online version of the article only. Users may download, print and share this work on the Internet for noncommercial purposes only, provided the original work is properly cited, and a link to the original work on http://www.karger.com and the terms of this license are included in any shared versions.
spellingShingle Published online: May, 2014
Shackelford, Rodney
Pollen, Maressa
Vora, Moise
Jusion, Tamara T.
Cotelingam, James
Nair, Binu
Malignant Melanoma with Concurrent BRAF E586K and NRAS Q81K Mutations
title Malignant Melanoma with Concurrent BRAF E586K and NRAS Q81K Mutations
title_full Malignant Melanoma with Concurrent BRAF E586K and NRAS Q81K Mutations
title_fullStr Malignant Melanoma with Concurrent BRAF E586K and NRAS Q81K Mutations
title_full_unstemmed Malignant Melanoma with Concurrent BRAF E586K and NRAS Q81K Mutations
title_short Malignant Melanoma with Concurrent BRAF E586K and NRAS Q81K Mutations
title_sort malignant melanoma with concurrent braf e586k and nras q81k mutations
topic Published online: May, 2014
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4035678/
https://www.ncbi.nlm.nih.gov/pubmed/24926260
http://dx.doi.org/10.1159/000362788
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