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Dermatofibrosarcoma protuberans in a young patient with epidermolysis bullosa: a case report

BACKGROUND: Epidermolysis bullosa is a group of rare inherited skin diseases characterized by blister formation following mechanical skin trauma. Epidermolysis bullosa is associated with increased skin cancer rates, predominantly squamous cell carcinomas, yet to our best knowledge, there is no repor...

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Autores principales: Bonaventura, B., Kraus, D., Stark, G. B., Fuellgraf, H., Kiefer, J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7903690/
https://www.ncbi.nlm.nih.gov/pubmed/33622311
http://dx.doi.org/10.1186/s12893-021-01105-6
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author Bonaventura, B.
Kraus, D.
Stark, G. B.
Fuellgraf, H.
Kiefer, J.
author_facet Bonaventura, B.
Kraus, D.
Stark, G. B.
Fuellgraf, H.
Kiefer, J.
author_sort Bonaventura, B.
collection PubMed
description BACKGROUND: Epidermolysis bullosa is a group of rare inherited skin diseases characterized by blister formation following mechanical skin trauma. Epidermolysis bullosa is associated with increased skin cancer rates, predominantly squamous cell carcinomas, yet to our best knowledge, there is no reported case of dermatofibrosarcoma protuberans in a patient with Epidermolysis bullosa. CASE PRESENTATION: Here, we present a 26-year-old man with junctional epidermolysis bullosa, who developed a DFSP on the neck. Initial, the skin alteration was mistakenly not considered malignant, which resulted in inadequate safety margins. The complete resection required a local flap to close the defect, which is not unproblematic because of the chronic inflammation and impaired healing potential of the skin due to Epidermolysis bullosa. CONCLUSIONS: To our best knowledge, this is the first reported case of a skin-associated sarcoma in a patient with EB; however, further investigation is required to verify a correlation.
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spelling pubmed-79036902021-03-01 Dermatofibrosarcoma protuberans in a young patient with epidermolysis bullosa: a case report Bonaventura, B. Kraus, D. Stark, G. B. Fuellgraf, H. Kiefer, J. BMC Surg Case Report BACKGROUND: Epidermolysis bullosa is a group of rare inherited skin diseases characterized by blister formation following mechanical skin trauma. Epidermolysis bullosa is associated with increased skin cancer rates, predominantly squamous cell carcinomas, yet to our best knowledge, there is no reported case of dermatofibrosarcoma protuberans in a patient with Epidermolysis bullosa. CASE PRESENTATION: Here, we present a 26-year-old man with junctional epidermolysis bullosa, who developed a DFSP on the neck. Initial, the skin alteration was mistakenly not considered malignant, which resulted in inadequate safety margins. The complete resection required a local flap to close the defect, which is not unproblematic because of the chronic inflammation and impaired healing potential of the skin due to Epidermolysis bullosa. CONCLUSIONS: To our best knowledge, this is the first reported case of a skin-associated sarcoma in a patient with EB; however, further investigation is required to verify a correlation. BioMed Central 2021-02-23 /pmc/articles/PMC7903690/ /pubmed/33622311 http://dx.doi.org/10.1186/s12893-021-01105-6 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Case Report
Bonaventura, B.
Kraus, D.
Stark, G. B.
Fuellgraf, H.
Kiefer, J.
Dermatofibrosarcoma protuberans in a young patient with epidermolysis bullosa: a case report
title Dermatofibrosarcoma protuberans in a young patient with epidermolysis bullosa: a case report
title_full Dermatofibrosarcoma protuberans in a young patient with epidermolysis bullosa: a case report
title_fullStr Dermatofibrosarcoma protuberans in a young patient with epidermolysis bullosa: a case report
title_full_unstemmed Dermatofibrosarcoma protuberans in a young patient with epidermolysis bullosa: a case report
title_short Dermatofibrosarcoma protuberans in a young patient with epidermolysis bullosa: a case report
title_sort dermatofibrosarcoma protuberans in a young patient with epidermolysis bullosa: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7903690/
https://www.ncbi.nlm.nih.gov/pubmed/33622311
http://dx.doi.org/10.1186/s12893-021-01105-6
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