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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...

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Autores principales: Nakajo, Kosuke, Iwai, Yoshiyasu, Yoshimura, Masaki, Watanabe, Yusuke, Yamanaka, Kazuhiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japan Neurosurgical Society 2019
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.
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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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