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Intracavernous Hemangiopericytoma: Case Report and Review of the Literature
Intracavernous hemangiopericytoma/solitary fibrous tumor is an extremely rare tumor, with only seven cases reported. We present a case of intracavernous hemangiopericytoma/solitary fibrous tumor and review all cases reported in the literature. A 67-year-old man experienced numbness over the left hal...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Japan Neurosurgical Society
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6776749/ https://www.ncbi.nlm.nih.gov/pubmed/31592158 http://dx.doi.org/10.2176/nmccrj.cr.2018-0300 |
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author | Nakajo, Kosuke Iwai, Yoshiyasu Yoshimura, Masaki Watanabe, Yusuke Yamanaka, Kazuhiro |
author_facet | Nakajo, Kosuke Iwai, Yoshiyasu Yoshimura, Masaki Watanabe, Yusuke Yamanaka, Kazuhiro |
author_sort | Nakajo, Kosuke |
collection | PubMed |
description | Intracavernous hemangiopericytoma/solitary fibrous tumor is an extremely rare tumor, with only seven cases reported. We present a case of intracavernous hemangiopericytoma/solitary fibrous tumor and review all cases reported in the literature. A 67-year-old man experienced numbness over the left half of the face. Magnetic resonance imaging revealed a left intracavernous tumor extending into Meckel’s cave and the posterior fossa. We performed gamma knife surgery (GKS) which a prescribed dose to the tumor of 12 Gy, but tumor recurred 43 months after GKS. We performed partial tumor resection via a subtemporal interdural approach. The pathological diagnosis was hemangiopericytoma. Postoperatively, we performed second GKS with a prescribed dose of 15 Gy. Diplopia and ptosis improved markedly and the tumor initially reduced in size, but tumor regrowth was seen again 29 months after second GKS. Third GKS was performed with a prescribed dose of 15 Gy. Recurrence was not seen at 18 months after third GKS, but was identified about 2 years after third GKS. We performed fourth GKS with a prescribed dose to the residual tumor of 16 Gy. We report a rare case of intracavernous hemangiopericytoma originating in the cavernous sinus, but distinguishing between hemangiopericytoma and schwannoma is difficult for round, intracavernous tumors showing homogeneous enhancement without flow voids. GKS might be one of the options for residual and recurrent intracavernous hemangiopericytomas. |
format | Online Article Text |
id | pubmed-6776749 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Japan Neurosurgical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-67767492019-10-07 Intracavernous Hemangiopericytoma: Case Report and Review of the Literature Nakajo, Kosuke Iwai, Yoshiyasu Yoshimura, Masaki Watanabe, Yusuke Yamanaka, Kazuhiro NMC Case Rep J Case Report Intracavernous hemangiopericytoma/solitary fibrous tumor is an extremely rare tumor, with only seven cases reported. We present a case of intracavernous hemangiopericytoma/solitary fibrous tumor and review all cases reported in the literature. A 67-year-old man experienced numbness over the left half of the face. Magnetic resonance imaging revealed a left intracavernous tumor extending into Meckel’s cave and the posterior fossa. We performed gamma knife surgery (GKS) which a prescribed dose to the tumor of 12 Gy, but tumor recurred 43 months after GKS. We performed partial tumor resection via a subtemporal interdural approach. The pathological diagnosis was hemangiopericytoma. Postoperatively, we performed second GKS with a prescribed dose of 15 Gy. Diplopia and ptosis improved markedly and the tumor initially reduced in size, but tumor regrowth was seen again 29 months after second GKS. Third GKS was performed with a prescribed dose of 15 Gy. Recurrence was not seen at 18 months after third GKS, but was identified about 2 years after third GKS. We performed fourth GKS with a prescribed dose to the residual tumor of 16 Gy. We report a rare case of intracavernous hemangiopericytoma originating in the cavernous sinus, but distinguishing between hemangiopericytoma and schwannoma is difficult for round, intracavernous tumors showing homogeneous enhancement without flow voids. GKS might be one of the options for residual and recurrent intracavernous hemangiopericytomas. The Japan Neurosurgical Society 2019-09-11 /pmc/articles/PMC6776749/ /pubmed/31592158 http://dx.doi.org/10.2176/nmccrj.cr.2018-0300 Text en © 2019 The Japan Neurosurgical Society This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/ |
spellingShingle | Case Report Nakajo, Kosuke Iwai, Yoshiyasu Yoshimura, Masaki Watanabe, Yusuke Yamanaka, Kazuhiro Intracavernous Hemangiopericytoma: Case Report and Review of the Literature |
title | Intracavernous Hemangiopericytoma: Case Report and Review of the Literature |
title_full | Intracavernous Hemangiopericytoma: Case Report and Review of the Literature |
title_fullStr | Intracavernous Hemangiopericytoma: Case Report and Review of the Literature |
title_full_unstemmed | Intracavernous Hemangiopericytoma: Case Report and Review of the Literature |
title_short | Intracavernous Hemangiopericytoma: Case Report and Review of the Literature |
title_sort | intracavernous hemangiopericytoma: case report and review of the literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6776749/ https://www.ncbi.nlm.nih.gov/pubmed/31592158 http://dx.doi.org/10.2176/nmccrj.cr.2018-0300 |
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