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Intracranial solitary fibrous tumor/hemangiopericytoma: Report of two cases and literature review
Intracranial solitary fibrous tumors (ISFTs) are rare mesenchymal neoplasms originating in the meninges and constitute a heterogeneous group of rare spindle cell tumors that include benign and malignant neoplasms of which hemangiopericytoma is nowadays considered a cellular phenotypic variant. ISFT...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Qassim Uninversity
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5604277/ https://www.ncbi.nlm.nih.gov/pubmed/28936155 |
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author | Aljohani, Hani Talal Chaussemy, D. Proust, F. Chibbaro, S. |
author_facet | Aljohani, Hani Talal Chaussemy, D. Proust, F. Chibbaro, S. |
author_sort | Aljohani, Hani Talal |
collection | PubMed |
description | Intracranial solitary fibrous tumors (ISFTs) are rare mesenchymal neoplasms originating in the meninges and constitute a heterogeneous group of rare spindle cell tumors that include benign and malignant neoplasms of which hemangiopericytoma is nowadays considered a cellular phenotypic variant. ISFT usually shows benign or indolent clinical behavior. We describe two cases of ISFT managed in our institution along with a review of pertinent literature. |
format | Online Article Text |
id | pubmed-5604277 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Qassim Uninversity |
record_format | MEDLINE/PubMed |
spelling | pubmed-56042772017-09-21 Intracranial solitary fibrous tumor/hemangiopericytoma: Report of two cases and literature review Aljohani, Hani Talal Chaussemy, D. Proust, F. Chibbaro, S. Int J Health Sci (Qassim) Case Report Intracranial solitary fibrous tumors (ISFTs) are rare mesenchymal neoplasms originating in the meninges and constitute a heterogeneous group of rare spindle cell tumors that include benign and malignant neoplasms of which hemangiopericytoma is nowadays considered a cellular phenotypic variant. ISFT usually shows benign or indolent clinical behavior. We describe two cases of ISFT managed in our institution along with a review of pertinent literature. Qassim Uninversity 2017 /pmc/articles/PMC5604277/ /pubmed/28936155 Text en Copyright: © International Journal of Health Sciences http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Aljohani, Hani Talal Chaussemy, D. Proust, F. Chibbaro, S. Intracranial solitary fibrous tumor/hemangiopericytoma: Report of two cases and literature review |
title | Intracranial solitary fibrous tumor/hemangiopericytoma: Report of two cases and literature review |
title_full | Intracranial solitary fibrous tumor/hemangiopericytoma: Report of two cases and literature review |
title_fullStr | Intracranial solitary fibrous tumor/hemangiopericytoma: Report of two cases and literature review |
title_full_unstemmed | Intracranial solitary fibrous tumor/hemangiopericytoma: Report of two cases and literature review |
title_short | Intracranial solitary fibrous tumor/hemangiopericytoma: Report of two cases and literature review |
title_sort | intracranial solitary fibrous tumor/hemangiopericytoma: report of two cases and literature review |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5604277/ https://www.ncbi.nlm.nih.gov/pubmed/28936155 |
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