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Giant cranionasal epithelioid haemangioendothelioma with invasive growth pattern mimicking a skull base chondrosarcoma
Epithelioid haemangioendothelioma (EHE) is a rare low-grade vascular neoplasm that is composed of mostly epithelioid cells. EHE may arise as a solitary tumour or in the form of multiple body lesions, and commonly occurs in soft tissues, liver, pleura, lung, peritoneum, lymph nodes, breast, and many...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Termedia Publishing House
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6103236/ https://www.ncbi.nlm.nih.gov/pubmed/30150890 http://dx.doi.org/10.5114/wo.2018.76235 |
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author | Batista, Kelvin Piña Gómez, Gonzalo Lepe Quintana, Eduardo Murias Astudillo, Aurora Fernandez-Vega, Ivan Fernandez, Belen Alvarez Cuellar-Martínez, Ana Llorente-Pendás, José Rovira-Pereira, Veronica Alvarez-Reyes, Kenia |
author_facet | Batista, Kelvin Piña Gómez, Gonzalo Lepe Quintana, Eduardo Murias Astudillo, Aurora Fernandez-Vega, Ivan Fernandez, Belen Alvarez Cuellar-Martínez, Ana Llorente-Pendás, José Rovira-Pereira, Veronica Alvarez-Reyes, Kenia |
author_sort | Batista, Kelvin Piña |
collection | PubMed |
description | Epithelioid haemangioendothelioma (EHE) is a rare low-grade vascular neoplasm that is composed of mostly epithelioid cells. EHE may arise as a solitary tumour or in the form of multiple body lesions, and commonly occurs in soft tissues, liver, pleura, lung, peritoneum, lymph nodes, breast, and many other sites. EHE in the cranionasal region is extremely rare. There are very few reports of cases of skull-base EHE. We discuss an extremely rare presentation of an aggressive EHE that originated from the sellar region. Based on literature review, our patient is the first reported case of a giant solitary EHE with prepontine cistern invasion and abducens nerve encroachment mimicking a chondrosarcoma. We treated this rare tumour by near subtotal surgical excision with subsequent radiotherapy, considering that complete tumour resection with free margins in both cavernous sinus and clival region avoiding neural and vascular structure encroachment becomes technically difficult. |
format | Online Article Text |
id | pubmed-6103236 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Termedia Publishing House |
record_format | MEDLINE/PubMed |
spelling | pubmed-61032362018-08-27 Giant cranionasal epithelioid haemangioendothelioma with invasive growth pattern mimicking a skull base chondrosarcoma Batista, Kelvin Piña Gómez, Gonzalo Lepe Quintana, Eduardo Murias Astudillo, Aurora Fernandez-Vega, Ivan Fernandez, Belen Alvarez Cuellar-Martínez, Ana Llorente-Pendás, José Rovira-Pereira, Veronica Alvarez-Reyes, Kenia Contemp Oncol (Pozn) Case Report Epithelioid haemangioendothelioma (EHE) is a rare low-grade vascular neoplasm that is composed of mostly epithelioid cells. EHE may arise as a solitary tumour or in the form of multiple body lesions, and commonly occurs in soft tissues, liver, pleura, lung, peritoneum, lymph nodes, breast, and many other sites. EHE in the cranionasal region is extremely rare. There are very few reports of cases of skull-base EHE. We discuss an extremely rare presentation of an aggressive EHE that originated from the sellar region. Based on literature review, our patient is the first reported case of a giant solitary EHE with prepontine cistern invasion and abducens nerve encroachment mimicking a chondrosarcoma. We treated this rare tumour by near subtotal surgical excision with subsequent radiotherapy, considering that complete tumour resection with free margins in both cavernous sinus and clival region avoiding neural and vascular structure encroachment becomes technically difficult. Termedia Publishing House 2018-06-13 2018 /pmc/articles/PMC6103236/ /pubmed/30150890 http://dx.doi.org/10.5114/wo.2018.76235 Text en Copyright: © 2018 Termedia Sp. z o. o. http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license. |
spellingShingle | Case Report Batista, Kelvin Piña Gómez, Gonzalo Lepe Quintana, Eduardo Murias Astudillo, Aurora Fernandez-Vega, Ivan Fernandez, Belen Alvarez Cuellar-Martínez, Ana Llorente-Pendás, José Rovira-Pereira, Veronica Alvarez-Reyes, Kenia Giant cranionasal epithelioid haemangioendothelioma with invasive growth pattern mimicking a skull base chondrosarcoma |
title | Giant cranionasal epithelioid haemangioendothelioma with invasive growth pattern mimicking a skull base chondrosarcoma |
title_full | Giant cranionasal epithelioid haemangioendothelioma with invasive growth pattern mimicking a skull base chondrosarcoma |
title_fullStr | Giant cranionasal epithelioid haemangioendothelioma with invasive growth pattern mimicking a skull base chondrosarcoma |
title_full_unstemmed | Giant cranionasal epithelioid haemangioendothelioma with invasive growth pattern mimicking a skull base chondrosarcoma |
title_short | Giant cranionasal epithelioid haemangioendothelioma with invasive growth pattern mimicking a skull base chondrosarcoma |
title_sort | giant cranionasal epithelioid haemangioendothelioma with invasive growth pattern mimicking a skull base chondrosarcoma |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6103236/ https://www.ncbi.nlm.nih.gov/pubmed/30150890 http://dx.doi.org/10.5114/wo.2018.76235 |
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