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Epithelioid angiosarcoma arising in a uterine leiomyoma with associated elevated CA-125: A case report
We describe the case of a 67 year old female with longstanding uterine leiomyomas who presented with fatigue, weight loss, elevated CA-125 and an enlarging mass arising from the posterior uterine fundus. Histologic sections of the mass contained a leiomyoma with interspersed foci of malignant epithe...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5430145/ https://www.ncbi.nlm.nih.gov/pubmed/28540360 http://dx.doi.org/10.1016/j.gore.2017.05.001 |
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author | Strickland, Sarah V. Kilgore, Mark R. Simons, Elise J. Rendi, Mara H. |
author_facet | Strickland, Sarah V. Kilgore, Mark R. Simons, Elise J. Rendi, Mara H. |
author_sort | Strickland, Sarah V. |
collection | PubMed |
description | We describe the case of a 67 year old female with longstanding uterine leiomyomas who presented with fatigue, weight loss, elevated CA-125 and an enlarging mass arising from the posterior uterine fundus. Histologic sections of the mass contained a leiomyoma with interspersed foci of malignant epithelioid cells forming anastomosing vascular channels. The neoplastic cells were diffusely positive for CD31 and FLI1, supporting the morphologic impression of epithelioid angiosarcoma. Few cases of epithelioid angiosarcoma arising within a leiomyoma have been described. In this report we discuss this association and describe its relation with elevated CA-125. |
format | Online Article Text |
id | pubmed-5430145 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-54301452017-05-24 Epithelioid angiosarcoma arising in a uterine leiomyoma with associated elevated CA-125: A case report Strickland, Sarah V. Kilgore, Mark R. Simons, Elise J. Rendi, Mara H. Gynecol Oncol Rep Case Report We describe the case of a 67 year old female with longstanding uterine leiomyomas who presented with fatigue, weight loss, elevated CA-125 and an enlarging mass arising from the posterior uterine fundus. Histologic sections of the mass contained a leiomyoma with interspersed foci of malignant epithelioid cells forming anastomosing vascular channels. The neoplastic cells were diffusely positive for CD31 and FLI1, supporting the morphologic impression of epithelioid angiosarcoma. Few cases of epithelioid angiosarcoma arising within a leiomyoma have been described. In this report we discuss this association and describe its relation with elevated CA-125. Elsevier 2017-05-05 /pmc/articles/PMC5430145/ /pubmed/28540360 http://dx.doi.org/10.1016/j.gore.2017.05.001 Text en © 2017 The Authors 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 Strickland, Sarah V. Kilgore, Mark R. Simons, Elise J. Rendi, Mara H. Epithelioid angiosarcoma arising in a uterine leiomyoma with associated elevated CA-125: A case report |
title | Epithelioid angiosarcoma arising in a uterine leiomyoma with associated elevated CA-125: A case report |
title_full | Epithelioid angiosarcoma arising in a uterine leiomyoma with associated elevated CA-125: A case report |
title_fullStr | Epithelioid angiosarcoma arising in a uterine leiomyoma with associated elevated CA-125: A case report |
title_full_unstemmed | Epithelioid angiosarcoma arising in a uterine leiomyoma with associated elevated CA-125: A case report |
title_short | Epithelioid angiosarcoma arising in a uterine leiomyoma with associated elevated CA-125: A case report |
title_sort | epithelioid angiosarcoma arising in a uterine leiomyoma with associated elevated ca-125: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5430145/ https://www.ncbi.nlm.nih.gov/pubmed/28540360 http://dx.doi.org/10.1016/j.gore.2017.05.001 |
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