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Nonmelanoma Skin Cancers: Embryologically Relevant Sites and UV Exposure
BACKGROUND: Traditionally, nonmelanoma skin cancers (NMSCs) are considered mainly UV-related malignancies. Nevertheless, a strong correlation between the embryologically relevant sites (ERS) of the head and neck and the preferential sites of onset of basal cell carcinomas (BCCs) has long been suppos...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7209852/ https://www.ncbi.nlm.nih.gov/pubmed/32440398 http://dx.doi.org/10.1097/GOX.0000000000002683 |
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author | Nicoletti, Giovanni Tresoldi, Marco Mario Malovini, Alberto Francesco, Borelli Faga, Angela |
author_facet | Nicoletti, Giovanni Tresoldi, Marco Mario Malovini, Alberto Francesco, Borelli Faga, Angela |
author_sort | Nicoletti, Giovanni |
collection | PubMed |
description | BACKGROUND: Traditionally, nonmelanoma skin cancers (NMSCs) are considered mainly UV-related malignancies. Nevertheless, a strong correlation between the embryologically relevant sites (ERS) of the head and neck and the preferential sites of onset of basal cell carcinomas (BCCs) has long been supposed and demonstrated. The aim of this research was the investigation of the potential correlation between the ERS of the head and neck and the sites of tumor onset in all of the NMSCs. METHODS: The distribution of 1165 NMSC was correlated with the ERS of the head and neck using the universally accepted anatomical diagrams featuring the congenital head and neck clefts and an original anatomical diagram showing the most credited sites of the embryonic fusion planes of the auricle. RESULTS: In our sample, both BCC and SSC display an increased likelihood of onset in the ERS of the head and neck. A proportion of 93.10% BCCs was distributed within ERS, while 6.90% derived from non-embryologically relevant sites (P < 0.001). A proportion of 69.70% SCCs was distributed within ERS, while 30.30% derived from non-embryologically relevant sites (P < 0.001). The probability of tumors within ERS was significantly higher for BCC versus SCC (P < 0.001), with BCCs having a 5-fold increase in the probability of occurring in ERS compared to SCCs (P < 0.001). CONCLUSIONS: The ERS might host areas of cellular instability yielding to the development of an NMSC. The environmental UV exposure plays a relatively main role versus dysontogenic factors in the pathogenesis of SCC. |
format | Online Article Text |
id | pubmed-7209852 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-72098522020-05-21 Nonmelanoma Skin Cancers: Embryologically Relevant Sites and UV Exposure Nicoletti, Giovanni Tresoldi, Marco Mario Malovini, Alberto Francesco, Borelli Faga, Angela Plast Reconstr Surg Glob Open Original Article BACKGROUND: Traditionally, nonmelanoma skin cancers (NMSCs) are considered mainly UV-related malignancies. Nevertheless, a strong correlation between the embryologically relevant sites (ERS) of the head and neck and the preferential sites of onset of basal cell carcinomas (BCCs) has long been supposed and demonstrated. The aim of this research was the investigation of the potential correlation between the ERS of the head and neck and the sites of tumor onset in all of the NMSCs. METHODS: The distribution of 1165 NMSC was correlated with the ERS of the head and neck using the universally accepted anatomical diagrams featuring the congenital head and neck clefts and an original anatomical diagram showing the most credited sites of the embryonic fusion planes of the auricle. RESULTS: In our sample, both BCC and SSC display an increased likelihood of onset in the ERS of the head and neck. A proportion of 93.10% BCCs was distributed within ERS, while 6.90% derived from non-embryologically relevant sites (P < 0.001). A proportion of 69.70% SCCs was distributed within ERS, while 30.30% derived from non-embryologically relevant sites (P < 0.001). The probability of tumors within ERS was significantly higher for BCC versus SCC (P < 0.001), with BCCs having a 5-fold increase in the probability of occurring in ERS compared to SCCs (P < 0.001). CONCLUSIONS: The ERS might host areas of cellular instability yielding to the development of an NMSC. The environmental UV exposure plays a relatively main role versus dysontogenic factors in the pathogenesis of SCC. Wolters Kluwer Health 2020-04-07 /pmc/articles/PMC7209852/ /pubmed/32440398 http://dx.doi.org/10.1097/GOX.0000000000002683 Text en Copyright © 2020 The Authors. Published by Wolters Kluwer Health, Inc. on behalf of The American Society of Plastic Surgeons. This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. |
spellingShingle | Original Article Nicoletti, Giovanni Tresoldi, Marco Mario Malovini, Alberto Francesco, Borelli Faga, Angela Nonmelanoma Skin Cancers: Embryologically Relevant Sites and UV Exposure |
title | Nonmelanoma Skin Cancers: Embryologically Relevant Sites and UV Exposure |
title_full | Nonmelanoma Skin Cancers: Embryologically Relevant Sites and UV Exposure |
title_fullStr | Nonmelanoma Skin Cancers: Embryologically Relevant Sites and UV Exposure |
title_full_unstemmed | Nonmelanoma Skin Cancers: Embryologically Relevant Sites and UV Exposure |
title_short | Nonmelanoma Skin Cancers: Embryologically Relevant Sites and UV Exposure |
title_sort | nonmelanoma skin cancers: embryologically relevant sites and uv exposure |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7209852/ https://www.ncbi.nlm.nih.gov/pubmed/32440398 http://dx.doi.org/10.1097/GOX.0000000000002683 |
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