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Supratentorial hemangioblastoma: A rare case report and literature review
Hemangioblastomas are rare and benign tumors of the central nervous system. They account for 1.5%-2.5% of all intracranial tumors and have an incidence of 3.2%. The resemblance of hemangioblastomas to other tumors renders preoperative diagnosis and management challenging. Herein, we report a case of...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9464762/ https://www.ncbi.nlm.nih.gov/pubmed/36105844 http://dx.doi.org/10.1016/j.radcr.2022.07.014 |
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author | Chang, Kai-Chieh Hsieh, Cheng-Ta Huang, Jing-Shan |
author_facet | Chang, Kai-Chieh Hsieh, Cheng-Ta Huang, Jing-Shan |
author_sort | Chang, Kai-Chieh |
collection | PubMed |
description | Hemangioblastomas are rare and benign tumors of the central nervous system. They account for 1.5%-2.5% of all intracranial tumors and have an incidence of 3.2%. The resemblance of hemangioblastomas to other tumors renders preoperative diagnosis and management challenging. Herein, we report a case of a supratentorial hemangioblastoma accompanied by extensive reactive gliosis and diagnosed through magnetic resonance imaging. In addition, we review the relevant literature. |
format | Online Article Text |
id | pubmed-9464762 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-94647622022-09-13 Supratentorial hemangioblastoma: A rare case report and literature review Chang, Kai-Chieh Hsieh, Cheng-Ta Huang, Jing-Shan Radiol Case Rep Case Report Hemangioblastomas are rare and benign tumors of the central nervous system. They account for 1.5%-2.5% of all intracranial tumors and have an incidence of 3.2%. The resemblance of hemangioblastomas to other tumors renders preoperative diagnosis and management challenging. Herein, we report a case of a supratentorial hemangioblastoma accompanied by extensive reactive gliosis and diagnosed through magnetic resonance imaging. In addition, we review the relevant literature. Elsevier 2022-09-06 /pmc/articles/PMC9464762/ /pubmed/36105844 http://dx.doi.org/10.1016/j.radcr.2022.07.014 Text en © 2022 The Authors. Published by Elsevier Inc. on behalf of University of Washington. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Case Report Chang, Kai-Chieh Hsieh, Cheng-Ta Huang, Jing-Shan Supratentorial hemangioblastoma: A rare case report and literature review |
title | Supratentorial hemangioblastoma: A rare case report and literature review |
title_full | Supratentorial hemangioblastoma: A rare case report and literature review |
title_fullStr | Supratentorial hemangioblastoma: A rare case report and literature review |
title_full_unstemmed | Supratentorial hemangioblastoma: A rare case report and literature review |
title_short | Supratentorial hemangioblastoma: A rare case report and literature review |
title_sort | supratentorial hemangioblastoma: a rare case report and literature review |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9464762/ https://www.ncbi.nlm.nih.gov/pubmed/36105844 http://dx.doi.org/10.1016/j.radcr.2022.07.014 |
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