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Photodynamic Therapy for Basal Cell Carcinoma in Recessive Dystrophic Epidermolysis Bullosa

A 22-year-old male with recessive dystrophic epidermolysis bullosa with a large superficial and nodular basal cell carcinoma on his right forehead was treated with photodynamic therapy. The treatment was well tolerated, and the site healed well. Patients with epidermolysis bullosa are at increased r...

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Detalles Bibliográficos
Autores principales: Lee, Myn Wee, Varigos, George, Foley, Peter, Ross, Gayle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scholarly Research Network 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3262548/
https://www.ncbi.nlm.nih.gov/pubmed/22363848
http://dx.doi.org/10.5402/2011/346754
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author Lee, Myn Wee
Varigos, George
Foley, Peter
Ross, Gayle
author_facet Lee, Myn Wee
Varigos, George
Foley, Peter
Ross, Gayle
author_sort Lee, Myn Wee
collection PubMed
description A 22-year-old male with recessive dystrophic epidermolysis bullosa with a large superficial and nodular basal cell carcinoma on his right forehead was treated with photodynamic therapy. The treatment was well tolerated, and the site healed well. Patients with epidermolysis bullosa are at increased risk of developing skin cancers, particularly squamous cell carcinomas. However, basal cell carcinomas are rare in recessive dystrophic epidermolysis bullosa. As patients with epidermolysis bullosa have recurrent blistering and poor wound healing, surgery may not be the optimal choice in treating skin cancers. We present this case to highlight that photodynamic therapy may be a helpful and safe technique in the treatment of superficial skin cancers in patients with epidermolysis bullosa, as an alternative to more radical methods.
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spelling pubmed-32625482012-02-23 Photodynamic Therapy for Basal Cell Carcinoma in Recessive Dystrophic Epidermolysis Bullosa Lee, Myn Wee Varigos, George Foley, Peter Ross, Gayle ISRN Dermatol Case Report A 22-year-old male with recessive dystrophic epidermolysis bullosa with a large superficial and nodular basal cell carcinoma on his right forehead was treated with photodynamic therapy. The treatment was well tolerated, and the site healed well. Patients with epidermolysis bullosa are at increased risk of developing skin cancers, particularly squamous cell carcinomas. However, basal cell carcinomas are rare in recessive dystrophic epidermolysis bullosa. As patients with epidermolysis bullosa have recurrent blistering and poor wound healing, surgery may not be the optimal choice in treating skin cancers. We present this case to highlight that photodynamic therapy may be a helpful and safe technique in the treatment of superficial skin cancers in patients with epidermolysis bullosa, as an alternative to more radical methods. International Scholarly Research Network 2011 2011-04-27 /pmc/articles/PMC3262548/ /pubmed/22363848 http://dx.doi.org/10.5402/2011/346754 Text en Copyright © 2011 Myn Wee Lee et al. 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
Lee, Myn Wee
Varigos, George
Foley, Peter
Ross, Gayle
Photodynamic Therapy for Basal Cell Carcinoma in Recessive Dystrophic Epidermolysis Bullosa
title Photodynamic Therapy for Basal Cell Carcinoma in Recessive Dystrophic Epidermolysis Bullosa
title_full Photodynamic Therapy for Basal Cell Carcinoma in Recessive Dystrophic Epidermolysis Bullosa
title_fullStr Photodynamic Therapy for Basal Cell Carcinoma in Recessive Dystrophic Epidermolysis Bullosa
title_full_unstemmed Photodynamic Therapy for Basal Cell Carcinoma in Recessive Dystrophic Epidermolysis Bullosa
title_short Photodynamic Therapy for Basal Cell Carcinoma in Recessive Dystrophic Epidermolysis Bullosa
title_sort photodynamic therapy for basal cell carcinoma in recessive dystrophic epidermolysis bullosa
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3262548/
https://www.ncbi.nlm.nih.gov/pubmed/22363848
http://dx.doi.org/10.5402/2011/346754
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