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Vaginal epithelioid angiosarcoma: A literature review of a rare entity in an unusual site

We describe an extremely rare case of a 66-year-old woman with a vaginal epithelioid angiosarcoma. She presented with constitutional symptoms, pelvic pain, vaginal bleeding, and a violaceous vaginal lesion. A thorough gynaecological examination, tissue biopsy and imaging were crucial to establish an...

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Detalles Bibliográficos
Autores principales: Weishaupt, J., Miller, J., Oehler, M.K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7873630/
https://www.ncbi.nlm.nih.gov/pubmed/33604443
http://dx.doi.org/10.1016/j.gore.2021.100706
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author Weishaupt, J.
Miller, J.
Oehler, M.K.
author_facet Weishaupt, J.
Miller, J.
Oehler, M.K.
author_sort Weishaupt, J.
collection PubMed
description We describe an extremely rare case of a 66-year-old woman with a vaginal epithelioid angiosarcoma. She presented with constitutional symptoms, pelvic pain, vaginal bleeding, and a violaceous vaginal lesion. A thorough gynaecological examination, tissue biopsy and imaging were crucial to establish an accurate diagnosis. With only 3 other cases reported in the literature, epithelioid angiosarcoma of the vagina seem to present late due to their nonspecific presentation and secluded location. Once diagnosed, optimal treatment is difficult to determine and together with the overly aggressive behaviour of these tumours, they are associated with a poor prognosis. To our knowledge, our case study and systematic literature review is the first to compare the management outcomes of epithelioid subtype angiosarcomas of the vagina. The rarity of this pathology contributes to diagnostic difficulties and lack of consensus regarding treatment of angiosarcomas of the vagina.
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spelling pubmed-78736302021-02-17 Vaginal epithelioid angiosarcoma: A literature review of a rare entity in an unusual site Weishaupt, J. Miller, J. Oehler, M.K. Gynecol Oncol Rep Case Report We describe an extremely rare case of a 66-year-old woman with a vaginal epithelioid angiosarcoma. She presented with constitutional symptoms, pelvic pain, vaginal bleeding, and a violaceous vaginal lesion. A thorough gynaecological examination, tissue biopsy and imaging were crucial to establish an accurate diagnosis. With only 3 other cases reported in the literature, epithelioid angiosarcoma of the vagina seem to present late due to their nonspecific presentation and secluded location. Once diagnosed, optimal treatment is difficult to determine and together with the overly aggressive behaviour of these tumours, they are associated with a poor prognosis. To our knowledge, our case study and systematic literature review is the first to compare the management outcomes of epithelioid subtype angiosarcomas of the vagina. The rarity of this pathology contributes to diagnostic difficulties and lack of consensus regarding treatment of angiosarcomas of the vagina. Elsevier 2021-01-21 /pmc/articles/PMC7873630/ /pubmed/33604443 http://dx.doi.org/10.1016/j.gore.2021.100706 Text en © 2021 The Authors. Published by Elsevier Inc. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Weishaupt, J.
Miller, J.
Oehler, M.K.
Vaginal epithelioid angiosarcoma: A literature review of a rare entity in an unusual site
title Vaginal epithelioid angiosarcoma: A literature review of a rare entity in an unusual site
title_full Vaginal epithelioid angiosarcoma: A literature review of a rare entity in an unusual site
title_fullStr Vaginal epithelioid angiosarcoma: A literature review of a rare entity in an unusual site
title_full_unstemmed Vaginal epithelioid angiosarcoma: A literature review of a rare entity in an unusual site
title_short Vaginal epithelioid angiosarcoma: A literature review of a rare entity in an unusual site
title_sort vaginal epithelioid angiosarcoma: a literature review of a rare entity in an unusual site
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7873630/
https://www.ncbi.nlm.nih.gov/pubmed/33604443
http://dx.doi.org/10.1016/j.gore.2021.100706
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