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Angiosarcoma of the Auricle in a Patient with Xeroderma Pigmentosum Variant
Xeroderma pigmentosum (XP) is an inherited autosomal recessive disorder characterized by photosensitivity and an increased risk of developing multiple skin neoplasms at sites exposed to the sun. We report a 73-year-old Japanese man with angiosarcoma of the auricle and an XP-variant, which is a very...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
S. Karger AG
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7506222/ https://www.ncbi.nlm.nih.gov/pubmed/32999650 http://dx.doi.org/10.1159/000508884 |
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author | Onishi, Masazumi Tsunoda, Kanako Maeda, Fumihiko Moriwaki, Shinichi Amano, Hiroo |
author_facet | Onishi, Masazumi Tsunoda, Kanako Maeda, Fumihiko Moriwaki, Shinichi Amano, Hiroo |
author_sort | Onishi, Masazumi |
collection | PubMed |
description | Xeroderma pigmentosum (XP) is an inherited autosomal recessive disorder characterized by photosensitivity and an increased risk of developing multiple skin neoplasms at sites exposed to the sun. We report a 73-year-old Japanese man with angiosarcoma of the auricle and an XP-variant, which is a very rare condition. In this case, long-term physical stimulation due to auricular deformation after surgery may have been the cause. Angiosarcoma associated with XP has a better prognosis than common angiosarcoma, perhaps because of the smaller tumor size. As XP patients are at high risk of skin neoplasms, they consult dermatologists regularly, and therefore skin tumors are likely to be detected early. |
format | Online Article Text |
id | pubmed-7506222 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | S. Karger AG |
record_format | MEDLINE/PubMed |
spelling | pubmed-75062222020-09-29 Angiosarcoma of the Auricle in a Patient with Xeroderma Pigmentosum Variant Onishi, Masazumi Tsunoda, Kanako Maeda, Fumihiko Moriwaki, Shinichi Amano, Hiroo Case Rep Dermatol Single Case Xeroderma pigmentosum (XP) is an inherited autosomal recessive disorder characterized by photosensitivity and an increased risk of developing multiple skin neoplasms at sites exposed to the sun. We report a 73-year-old Japanese man with angiosarcoma of the auricle and an XP-variant, which is a very rare condition. In this case, long-term physical stimulation due to auricular deformation after surgery may have been the cause. Angiosarcoma associated with XP has a better prognosis than common angiosarcoma, perhaps because of the smaller tumor size. As XP patients are at high risk of skin neoplasms, they consult dermatologists regularly, and therefore skin tumors are likely to be detected early. S. Karger AG 2020-08-18 /pmc/articles/PMC7506222/ /pubmed/32999650 http://dx.doi.org/10.1159/000508884 Text en Copyright © 2020 by S. Karger AG, Basel http://creativecommons.org/licenses/by-nc/4.0/ This article is licensed under the Creative Commons Attribution-NonCommercial-4.0 International License (CC BY-NC) (http://www.karger.com/Services/OpenAccessLicense). Usage and distribution for commercial purposes requires written permission. |
spellingShingle | Single Case Onishi, Masazumi Tsunoda, Kanako Maeda, Fumihiko Moriwaki, Shinichi Amano, Hiroo Angiosarcoma of the Auricle in a Patient with Xeroderma Pigmentosum Variant |
title | Angiosarcoma of the Auricle in a Patient with Xeroderma Pigmentosum Variant |
title_full | Angiosarcoma of the Auricle in a Patient with Xeroderma Pigmentosum Variant |
title_fullStr | Angiosarcoma of the Auricle in a Patient with Xeroderma Pigmentosum Variant |
title_full_unstemmed | Angiosarcoma of the Auricle in a Patient with Xeroderma Pigmentosum Variant |
title_short | Angiosarcoma of the Auricle in a Patient with Xeroderma Pigmentosum Variant |
title_sort | angiosarcoma of the auricle in a patient with xeroderma pigmentosum variant |
topic | Single Case |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7506222/ https://www.ncbi.nlm.nih.gov/pubmed/32999650 http://dx.doi.org/10.1159/000508884 |
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