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Clinical and dermoscopic stability and volatility of melanocytic nevi in a population-based cohort of children in Framingham school system

Nevi are important risk markers of melanoma. The study aim was to describe changes in nevi of children using longitudinal data from a population-based cohort. Overview back photography and dermoscopic imaging of up to 4 index back nevi was performed at age 11 (baseline) and repeated at age 14 (follo...

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Autores principales: Scope, Alon, Dusza, Stephen W., Marghoob, Ashfaq A., Satagopan, Jaya M., Braga, Casagrande Tavoloni Juliana, Psaty, Estee L., Weinstock, Martin A., Oliveria, Susan A., Bishop, Marilyn, Geller, Alan C., Halpern, Allan C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3136658/
https://www.ncbi.nlm.nih.gov/pubmed/21562569
http://dx.doi.org/10.1038/jid.2011.107
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author Scope, Alon
Dusza, Stephen W.
Marghoob, Ashfaq A.
Satagopan, Jaya M.
Braga, Casagrande Tavoloni Juliana
Psaty, Estee L.
Weinstock, Martin A.
Oliveria, Susan A.
Bishop, Marilyn
Geller, Alan C.
Halpern, Allan C.
author_facet Scope, Alon
Dusza, Stephen W.
Marghoob, Ashfaq A.
Satagopan, Jaya M.
Braga, Casagrande Tavoloni Juliana
Psaty, Estee L.
Weinstock, Martin A.
Oliveria, Susan A.
Bishop, Marilyn
Geller, Alan C.
Halpern, Allan C.
author_sort Scope, Alon
collection PubMed
description Nevi are important risk markers of melanoma. The study aim was to describe changes in nevi of children using longitudinal data from a population-based cohort. Overview back photography and dermoscopic imaging of up to 4 index back nevi was performed at age 11 (baseline) and repeated at age 14 (follow-up). Of 443 children (39% females) imaged at baseline, 366 children (39% females) had repeated imaging three year later. At age 14, median back nevus counts increased by 2; 75% of students (n=274) had at least one new back nevus and 28% (n=103) had at least one nevus that disappeared. Of 936 index nevi imaged dermoscopically at baseline and follow-up, 69% (645 nevi) had retained the same dermoscopic classification from baseline evaluation. Only 4% (n=13) of nevi assessed as globular at baseline were classified as reticular at follow-up, and just 3% (n=3) of baseline reticular nevi were classified as globular at follow-up. Of 9 (1%) index nevi that disappeared at follow-up, none showed halo or regression at baseline. In conclusion, the relative stability of dermoscopic pattern of individual nevi in the face of the overall volatility of nevi during adolescence suggests that specific dermoscopic patterns may represent distinct biologic nevus subsets.
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spelling pubmed-31366582012-02-01 Clinical and dermoscopic stability and volatility of melanocytic nevi in a population-based cohort of children in Framingham school system Scope, Alon Dusza, Stephen W. Marghoob, Ashfaq A. Satagopan, Jaya M. Braga, Casagrande Tavoloni Juliana Psaty, Estee L. Weinstock, Martin A. Oliveria, Susan A. Bishop, Marilyn Geller, Alan C. Halpern, Allan C. J Invest Dermatol Article Nevi are important risk markers of melanoma. The study aim was to describe changes in nevi of children using longitudinal data from a population-based cohort. Overview back photography and dermoscopic imaging of up to 4 index back nevi was performed at age 11 (baseline) and repeated at age 14 (follow-up). Of 443 children (39% females) imaged at baseline, 366 children (39% females) had repeated imaging three year later. At age 14, median back nevus counts increased by 2; 75% of students (n=274) had at least one new back nevus and 28% (n=103) had at least one nevus that disappeared. Of 936 index nevi imaged dermoscopically at baseline and follow-up, 69% (645 nevi) had retained the same dermoscopic classification from baseline evaluation. Only 4% (n=13) of nevi assessed as globular at baseline were classified as reticular at follow-up, and just 3% (n=3) of baseline reticular nevi were classified as globular at follow-up. Of 9 (1%) index nevi that disappeared at follow-up, none showed halo or regression at baseline. In conclusion, the relative stability of dermoscopic pattern of individual nevi in the face of the overall volatility of nevi during adolescence suggests that specific dermoscopic patterns may represent distinct biologic nevus subsets. 2011-05-12 2011-08 /pmc/articles/PMC3136658/ /pubmed/21562569 http://dx.doi.org/10.1038/jid.2011.107 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Scope, Alon
Dusza, Stephen W.
Marghoob, Ashfaq A.
Satagopan, Jaya M.
Braga, Casagrande Tavoloni Juliana
Psaty, Estee L.
Weinstock, Martin A.
Oliveria, Susan A.
Bishop, Marilyn
Geller, Alan C.
Halpern, Allan C.
Clinical and dermoscopic stability and volatility of melanocytic nevi in a population-based cohort of children in Framingham school system
title Clinical and dermoscopic stability and volatility of melanocytic nevi in a population-based cohort of children in Framingham school system
title_full Clinical and dermoscopic stability and volatility of melanocytic nevi in a population-based cohort of children in Framingham school system
title_fullStr Clinical and dermoscopic stability and volatility of melanocytic nevi in a population-based cohort of children in Framingham school system
title_full_unstemmed Clinical and dermoscopic stability and volatility of melanocytic nevi in a population-based cohort of children in Framingham school system
title_short Clinical and dermoscopic stability and volatility of melanocytic nevi in a population-based cohort of children in Framingham school system
title_sort clinical and dermoscopic stability and volatility of melanocytic nevi in a population-based cohort of children in framingham school system
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3136658/
https://www.ncbi.nlm.nih.gov/pubmed/21562569
http://dx.doi.org/10.1038/jid.2011.107
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