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Cutaneous Angiosarcoma of Head and Neck

Cutaneous angiosarcoma is a rare aggressive tumor of capillary and lymphatic endothelial cell origin. Cutaneous angiosarcoma of the head and neck regions seems to be a distinctive neoplasm with characteristic clinicopathologic features that differ from angiosarcoma in other anatomic locations. Angio...

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Autores principales: Vora, Rita, Anjaneyan, Gopikrishnan, Gupta, Rajat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4248527/
https://www.ncbi.nlm.nih.gov/pubmed/25484419
http://dx.doi.org/10.4103/0019-5154.143575
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author Vora, Rita
Anjaneyan, Gopikrishnan
Gupta, Rajat
author_facet Vora, Rita
Anjaneyan, Gopikrishnan
Gupta, Rajat
author_sort Vora, Rita
collection PubMed
description Cutaneous angiosarcoma is a rare aggressive tumor of capillary and lymphatic endothelial cell origin. Cutaneous angiosarcoma of the head and neck regions seems to be a distinctive neoplasm with characteristic clinicopathologic features that differ from angiosarcoma in other anatomic locations. Angiosarcoma, regardless of their setting, has a bad prognosis. We presented here a case of 80 years old male, with multiple nontender grouped purple to red hemorrhagic vesicular and bullous lesions over left lower cheek and upper neck area, with bilateral cervical lymph nodes since 1 month. Computed tomography thorax showed nodular opacities in the right upper and midzones. Excisional biopsy showed characterstic “dissection of collagen” with mild nuclear atypia. Immunohistochemistry showed tumor cell positive for CD-31 and Fli-1. Patient died within 1 month of presentation.
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spelling pubmed-42485272014-12-05 Cutaneous Angiosarcoma of Head and Neck Vora, Rita Anjaneyan, Gopikrishnan Gupta, Rajat Indian J Dermatol E-IJD Case Report Cutaneous angiosarcoma is a rare aggressive tumor of capillary and lymphatic endothelial cell origin. Cutaneous angiosarcoma of the head and neck regions seems to be a distinctive neoplasm with characteristic clinicopathologic features that differ from angiosarcoma in other anatomic locations. Angiosarcoma, regardless of their setting, has a bad prognosis. We presented here a case of 80 years old male, with multiple nontender grouped purple to red hemorrhagic vesicular and bullous lesions over left lower cheek and upper neck area, with bilateral cervical lymph nodes since 1 month. Computed tomography thorax showed nodular opacities in the right upper and midzones. Excisional biopsy showed characterstic “dissection of collagen” with mild nuclear atypia. Immunohistochemistry showed tumor cell positive for CD-31 and Fli-1. Patient died within 1 month of presentation. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC4248527/ /pubmed/25484419 http://dx.doi.org/10.4103/0019-5154.143575 Text en Copyright: © Indian Journal of Dermatology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle E-IJD Case Report
Vora, Rita
Anjaneyan, Gopikrishnan
Gupta, Rajat
Cutaneous Angiosarcoma of Head and Neck
title Cutaneous Angiosarcoma of Head and Neck
title_full Cutaneous Angiosarcoma of Head and Neck
title_fullStr Cutaneous Angiosarcoma of Head and Neck
title_full_unstemmed Cutaneous Angiosarcoma of Head and Neck
title_short Cutaneous Angiosarcoma of Head and Neck
title_sort cutaneous angiosarcoma of head and neck
topic E-IJD Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4248527/
https://www.ncbi.nlm.nih.gov/pubmed/25484419
http://dx.doi.org/10.4103/0019-5154.143575
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