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Suprasellar Benign Chondroma: A Case Report and Literature Review

Intracranial chondroma is a rare benign tumor comprising only 0.2% of all intracranial tumors. A 27-year-old woman presented with visual dysfunction and headache. Brain computed tomography and magnetic resonance imaging revealed a suprasellar mass lesion with a calcified component. Gross total remov...

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Autores principales: Nakanowatari, Satoshi, Sakata, Katsumi, Miyazaki, Ryohei, Kawasaki, Takashi, Manaka, Hiroshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japan Neurosurgical Society 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7162814/
https://www.ncbi.nlm.nih.gov/pubmed/32322453
http://dx.doi.org/10.2176/nmccrj.cr.2019-0136
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author Nakanowatari, Satoshi
Sakata, Katsumi
Miyazaki, Ryohei
Kawasaki, Takashi
Manaka, Hiroshi
author_facet Nakanowatari, Satoshi
Sakata, Katsumi
Miyazaki, Ryohei
Kawasaki, Takashi
Manaka, Hiroshi
author_sort Nakanowatari, Satoshi
collection PubMed
description Intracranial chondroma is a rare benign tumor comprising only 0.2% of all intracranial tumors. A 27-year-old woman presented with visual dysfunction and headache. Brain computed tomography and magnetic resonance imaging revealed a suprasellar mass lesion with a calcified component. Gross total removal was achieved via a basal interhemispheric approach. Postoperatively, visual function improved to the normal range, and no recurrence was evident 4 years later. Histopathological examination confirmed the diagnosis of benign chondroma. Preoperative differentiation of chondromas from chordomas is clinically important, because of the different treatment and prognostic implications. The only effective treatment for chondroma is total surgical removal. We present a case of gross total resection of a suprasellar chondroma with reference to the literature.
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spelling pubmed-71628142020-04-22 Suprasellar Benign Chondroma: A Case Report and Literature Review Nakanowatari, Satoshi Sakata, Katsumi Miyazaki, Ryohei Kawasaki, Takashi Manaka, Hiroshi NMC Case Rep J Case Report Intracranial chondroma is a rare benign tumor comprising only 0.2% of all intracranial tumors. A 27-year-old woman presented with visual dysfunction and headache. Brain computed tomography and magnetic resonance imaging revealed a suprasellar mass lesion with a calcified component. Gross total removal was achieved via a basal interhemispheric approach. Postoperatively, visual function improved to the normal range, and no recurrence was evident 4 years later. Histopathological examination confirmed the diagnosis of benign chondroma. Preoperative differentiation of chondromas from chordomas is clinically important, because of the different treatment and prognostic implications. The only effective treatment for chondroma is total surgical removal. We present a case of gross total resection of a suprasellar chondroma with reference to the literature. The Japan Neurosurgical Society 2020-03-24 /pmc/articles/PMC7162814/ /pubmed/32322453 http://dx.doi.org/10.2176/nmccrj.cr.2019-0136 Text en © 2020 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
Nakanowatari, Satoshi
Sakata, Katsumi
Miyazaki, Ryohei
Kawasaki, Takashi
Manaka, Hiroshi
Suprasellar Benign Chondroma: A Case Report and Literature Review
title Suprasellar Benign Chondroma: A Case Report and Literature Review
title_full Suprasellar Benign Chondroma: A Case Report and Literature Review
title_fullStr Suprasellar Benign Chondroma: A Case Report and Literature Review
title_full_unstemmed Suprasellar Benign Chondroma: A Case Report and Literature Review
title_short Suprasellar Benign Chondroma: A Case Report and Literature Review
title_sort suprasellar benign chondroma: a case report and literature review
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7162814/
https://www.ncbi.nlm.nih.gov/pubmed/32322453
http://dx.doi.org/10.2176/nmccrj.cr.2019-0136
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