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Complete regression of primary melanoma associated with nevi involution under BRAF inhibitors: A case report and review of the literature

Melanoma is one of the most immunogenic tumors among human neoplasms, with numerous clinical observations of partial or completely regressed tumors. It is an aggressive tumor, with the greatest reported number of somatic mutations, BRAF mutation being the most common one. BRAF mutation is also prese...

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Autores principales: Grigore, Lavinia Elena, Ungureanu, Loredana, Bejinariu, Nona, Seceac, Crina, Vasilovici, Alina, Senila, Simona Corina, Candrea, Elisabeta, Fechete, Oana, Cosgarea, Rodica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6444337/
https://www.ncbi.nlm.nih.gov/pubmed/30944613
http://dx.doi.org/10.3892/ol.2018.9738
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author Grigore, Lavinia Elena
Ungureanu, Loredana
Bejinariu, Nona
Seceac, Crina
Vasilovici, Alina
Senila, Simona Corina
Candrea, Elisabeta
Fechete, Oana
Cosgarea, Rodica
author_facet Grigore, Lavinia Elena
Ungureanu, Loredana
Bejinariu, Nona
Seceac, Crina
Vasilovici, Alina
Senila, Simona Corina
Candrea, Elisabeta
Fechete, Oana
Cosgarea, Rodica
author_sort Grigore, Lavinia Elena
collection PubMed
description Melanoma is one of the most immunogenic tumors among human neoplasms, with numerous clinical observations of partial or completely regressed tumors. It is an aggressive tumor, with the greatest reported number of somatic mutations, BRAF mutation being the most common one. BRAF mutation is also present in a higher percentage in benign nevi. Complete regression of primary tumor and involution of nevi are, however, rare phenomenon in melanoma that can appear in relation with UV exposure, surgical trauma, target therapy in melanoma, pregnancy or host immune response to an evolving melanoma tumor. We present the case of a 58-year-old man with a completely regressed metastatic melanoma who developed a second melanoma with concomitant involution of papillomatous nevi under BRAF inhibitors treatment. In reviewed literature we have found 53 cases of completely regressed primary melanomas, neither of them reporting nevi involution. Complete regression of primary tumor can occur as an immune response to tumor progression. Nevi can involute under BRAF inhibitor therapy, but development of new malignant lesions under BRAF inhibitors is linked to BRAF wild-type. Documentation of primary tumor and dynamic changes in nevi highlight the need of a good clinical skin examination and increase the utility of baseline and sequential dermoscopy in melanoma.
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spelling pubmed-64443372019-04-03 Complete regression of primary melanoma associated with nevi involution under BRAF inhibitors: A case report and review of the literature Grigore, Lavinia Elena Ungureanu, Loredana Bejinariu, Nona Seceac, Crina Vasilovici, Alina Senila, Simona Corina Candrea, Elisabeta Fechete, Oana Cosgarea, Rodica Oncol Lett Articles Melanoma is one of the most immunogenic tumors among human neoplasms, with numerous clinical observations of partial or completely regressed tumors. It is an aggressive tumor, with the greatest reported number of somatic mutations, BRAF mutation being the most common one. BRAF mutation is also present in a higher percentage in benign nevi. Complete regression of primary tumor and involution of nevi are, however, rare phenomenon in melanoma that can appear in relation with UV exposure, surgical trauma, target therapy in melanoma, pregnancy or host immune response to an evolving melanoma tumor. We present the case of a 58-year-old man with a completely regressed metastatic melanoma who developed a second melanoma with concomitant involution of papillomatous nevi under BRAF inhibitors treatment. In reviewed literature we have found 53 cases of completely regressed primary melanomas, neither of them reporting nevi involution. Complete regression of primary tumor can occur as an immune response to tumor progression. Nevi can involute under BRAF inhibitor therapy, but development of new malignant lesions under BRAF inhibitors is linked to BRAF wild-type. Documentation of primary tumor and dynamic changes in nevi highlight the need of a good clinical skin examination and increase the utility of baseline and sequential dermoscopy in melanoma. D.A. Spandidos 2019-05 2018-11-19 /pmc/articles/PMC6444337/ /pubmed/30944613 http://dx.doi.org/10.3892/ol.2018.9738 Text en Copyright: © Grigore et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Grigore, Lavinia Elena
Ungureanu, Loredana
Bejinariu, Nona
Seceac, Crina
Vasilovici, Alina
Senila, Simona Corina
Candrea, Elisabeta
Fechete, Oana
Cosgarea, Rodica
Complete regression of primary melanoma associated with nevi involution under BRAF inhibitors: A case report and review of the literature
title Complete regression of primary melanoma associated with nevi involution under BRAF inhibitors: A case report and review of the literature
title_full Complete regression of primary melanoma associated with nevi involution under BRAF inhibitors: A case report and review of the literature
title_fullStr Complete regression of primary melanoma associated with nevi involution under BRAF inhibitors: A case report and review of the literature
title_full_unstemmed Complete regression of primary melanoma associated with nevi involution under BRAF inhibitors: A case report and review of the literature
title_short Complete regression of primary melanoma associated with nevi involution under BRAF inhibitors: A case report and review of the literature
title_sort complete regression of primary melanoma associated with nevi involution under braf inhibitors: a case report and review of the literature
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6444337/
https://www.ncbi.nlm.nih.gov/pubmed/30944613
http://dx.doi.org/10.3892/ol.2018.9738
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