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Basal Cell Carcinoma in Type 2 Segmental Darier's Disease
Background. Darier's disease (DD), also known as Keratosis Follicularis or Darier-White disease, is a rare disorder of keratinization. DD can present as a generalized autosomal dominant condition as well as a localized or segmental postzygotic condition (Vázquez et al., 2002). Clinical features...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2012
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3150772/ https://www.ncbi.nlm.nih.gov/pubmed/21826272 http://dx.doi.org/10.1155/2012/839561 |
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author | Robertson, Lynne Sauder, Maxwell B. |
author_facet | Robertson, Lynne Sauder, Maxwell B. |
author_sort | Robertson, Lynne |
collection | PubMed |
description | Background. Darier's disease (DD), also known as Keratosis Follicularis or Darier-White disease, is a rare disorder of keratinization. DD can present as a generalized autosomal dominant condition as well as a localized or segmental postzygotic condition (Vázquez et al., 2002). Clinical features of DD include greasy, warty papules and plaques on seborrheic areas, dystrophic nails, palmo-plantar pits, and papules on the dorsum of the hands and feet. Objective. We report a case of basal cell carcinoma developing in a patient with type 2 segmental DD. Conclusion. According to the current literature, Type 2 segmental disease is a rare presentation of Darier's disease with only 8 previous cases reported to date. In addition, nonmelanoma skin cancer (NMSC) arising from DD is rarely reported; however, there may be an association between DD and risk of carcinogenesis. |
format | Online Article Text |
id | pubmed-3150772 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-31507722011-08-08 Basal Cell Carcinoma in Type 2 Segmental Darier's Disease Robertson, Lynne Sauder, Maxwell B. J Skin Cancer Case Report Background. Darier's disease (DD), also known as Keratosis Follicularis or Darier-White disease, is a rare disorder of keratinization. DD can present as a generalized autosomal dominant condition as well as a localized or segmental postzygotic condition (Vázquez et al., 2002). Clinical features of DD include greasy, warty papules and plaques on seborrheic areas, dystrophic nails, palmo-plantar pits, and papules on the dorsum of the hands and feet. Objective. We report a case of basal cell carcinoma developing in a patient with type 2 segmental DD. Conclusion. According to the current literature, Type 2 segmental disease is a rare presentation of Darier's disease with only 8 previous cases reported to date. In addition, nonmelanoma skin cancer (NMSC) arising from DD is rarely reported; however, there may be an association between DD and risk of carcinogenesis. Hindawi Publishing Corporation 2012 2011-07-31 /pmc/articles/PMC3150772/ /pubmed/21826272 http://dx.doi.org/10.1155/2012/839561 Text en Copyright © 2012 L. Robertson and M. B. Sauder. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Robertson, Lynne Sauder, Maxwell B. Basal Cell Carcinoma in Type 2 Segmental Darier's Disease |
title | Basal Cell Carcinoma in Type 2 Segmental Darier's Disease |
title_full | Basal Cell Carcinoma in Type 2 Segmental Darier's Disease |
title_fullStr | Basal Cell Carcinoma in Type 2 Segmental Darier's Disease |
title_full_unstemmed | Basal Cell Carcinoma in Type 2 Segmental Darier's Disease |
title_short | Basal Cell Carcinoma in Type 2 Segmental Darier's Disease |
title_sort | basal cell carcinoma in type 2 segmental darier's disease |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3150772/ https://www.ncbi.nlm.nih.gov/pubmed/21826272 http://dx.doi.org/10.1155/2012/839561 |
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