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Malignant perivascular epithelioid cell tumor of the uterus
Perivascular epithelioid cell tumors (PEComas) are a rare collection of tumors arising in a wide array of anatomic locations and characterized by a myomelanocytic phenotype. PEComas which occur in non-classic anatomic distributions are known as perivascular epithelioid cell tumor-not otherwise speci...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
PAGEPress Publications
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3325741/ https://www.ncbi.nlm.nih.gov/pubmed/22532912 http://dx.doi.org/10.4081/rt.2012.e14 |
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author | Bleeker, Jonathan S. Quevedo, J. Fernando Folpe, Andrew L. |
author_facet | Bleeker, Jonathan S. Quevedo, J. Fernando Folpe, Andrew L. |
author_sort | Bleeker, Jonathan S. |
collection | PubMed |
description | Perivascular epithelioid cell tumors (PEComas) are a rare collection of tumors arising in a wide array of anatomic locations and characterized by a myomelanocytic phenotype. PEComas which occur in non-classic anatomic distributions are known as perivascular epithelioid cell tumor-not otherwise specified (PEComa-NOS), and one of the most common primary sites for PEComa-NOS is the uterus. The risk of aggressive behavior of these tumors has been linked to a number of factors evaluable on pathologic review following initial surgical resection. We report a case of PEComa-NOS of the uterus with multiple high-risk features, including frank vascular invasion, with no evidence of recurrent disease 18 months following initial surgical resection. |
format | Online Article Text |
id | pubmed-3325741 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | PAGEPress Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-33257412012-04-24 Malignant perivascular epithelioid cell tumor of the uterus Bleeker, Jonathan S. Quevedo, J. Fernando Folpe, Andrew L. Rare Tumors Case Report Perivascular epithelioid cell tumors (PEComas) are a rare collection of tumors arising in a wide array of anatomic locations and characterized by a myomelanocytic phenotype. PEComas which occur in non-classic anatomic distributions are known as perivascular epithelioid cell tumor-not otherwise specified (PEComa-NOS), and one of the most common primary sites for PEComa-NOS is the uterus. The risk of aggressive behavior of these tumors has been linked to a number of factors evaluable on pathologic review following initial surgical resection. We report a case of PEComa-NOS of the uterus with multiple high-risk features, including frank vascular invasion, with no evidence of recurrent disease 18 months following initial surgical resection. PAGEPress Publications 2012-03-12 /pmc/articles/PMC3325741/ /pubmed/22532912 http://dx.doi.org/10.4081/rt.2012.e14 Text en ©Copyright J.S. Bleeker et al., 2012 This work is licensed under a Creative Commons Attribution NonCommercial 3.0 License (CC BY-NC 3.0). Licensee PAGEPress, Italy |
spellingShingle | Case Report Bleeker, Jonathan S. Quevedo, J. Fernando Folpe, Andrew L. Malignant perivascular epithelioid cell tumor of the uterus |
title | Malignant perivascular epithelioid cell tumor of the uterus |
title_full | Malignant perivascular epithelioid cell tumor of the uterus |
title_fullStr | Malignant perivascular epithelioid cell tumor of the uterus |
title_full_unstemmed | Malignant perivascular epithelioid cell tumor of the uterus |
title_short | Malignant perivascular epithelioid cell tumor of the uterus |
title_sort | malignant perivascular epithelioid cell tumor of the uterus |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3325741/ https://www.ncbi.nlm.nih.gov/pubmed/22532912 http://dx.doi.org/10.4081/rt.2012.e14 |
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