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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2018
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.
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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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