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Cerebellar hemangioblastoma: Case report with review of the literature
Originally recognized by Cushing and Bailey, hemangioblastoma is a developmental vascular neoplasm that is predominantly found in the posterior fossa. It is a highly vascularized tumor, with well-differentiated histologic features. Although rare, it remains the most common primary tumor of cerebellu...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8367806/ https://www.ncbi.nlm.nih.gov/pubmed/34429813 http://dx.doi.org/10.1016/j.radcr.2021.07.027 |
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author | Lahkim, Mohamed Andour, Hajar Laamrani, Fatima Zahrae Allaoui, Mohamed Saouab, Rachida El Fenni, Jamal En-Nouali, Hassan |
author_facet | Lahkim, Mohamed Andour, Hajar Laamrani, Fatima Zahrae Allaoui, Mohamed Saouab, Rachida El Fenni, Jamal En-Nouali, Hassan |
author_sort | Lahkim, Mohamed |
collection | PubMed |
description | Originally recognized by Cushing and Bailey, hemangioblastoma is a developmental vascular neoplasm that is predominantly found in the posterior fossa. It is a highly vascularized tumor, with well-differentiated histologic features. Although rare, it remains the most common primary tumor of cerebellum in adults, along with metastases. MRI is the gold standard, allowing a precise characterization of the lesion's features, and its relationship with the surrounding structures. We report the case of a patient with a cerebellar symptomatology, in whom brain MRI raises the diagnosis of hemangioblastoma, which was then confirmed by histopathologic examination. |
format | Online Article Text |
id | pubmed-8367806 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-83678062021-08-23 Cerebellar hemangioblastoma: Case report with review of the literature Lahkim, Mohamed Andour, Hajar Laamrani, Fatima Zahrae Allaoui, Mohamed Saouab, Rachida El Fenni, Jamal En-Nouali, Hassan Radiol Case Rep Case Report Originally recognized by Cushing and Bailey, hemangioblastoma is a developmental vascular neoplasm that is predominantly found in the posterior fossa. It is a highly vascularized tumor, with well-differentiated histologic features. Although rare, it remains the most common primary tumor of cerebellum in adults, along with metastases. MRI is the gold standard, allowing a precise characterization of the lesion's features, and its relationship with the surrounding structures. We report the case of a patient with a cerebellar symptomatology, in whom brain MRI raises the diagnosis of hemangioblastoma, which was then confirmed by histopathologic examination. Elsevier 2021-08-14 /pmc/articles/PMC8367806/ /pubmed/34429813 http://dx.doi.org/10.1016/j.radcr.2021.07.027 Text en © 2021 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 Lahkim, Mohamed Andour, Hajar Laamrani, Fatima Zahrae Allaoui, Mohamed Saouab, Rachida El Fenni, Jamal En-Nouali, Hassan Cerebellar hemangioblastoma: Case report with review of the literature |
title | Cerebellar hemangioblastoma: Case report with review of the literature |
title_full | Cerebellar hemangioblastoma: Case report with review of the literature |
title_fullStr | Cerebellar hemangioblastoma: Case report with review of the literature |
title_full_unstemmed | Cerebellar hemangioblastoma: Case report with review of the literature |
title_short | Cerebellar hemangioblastoma: Case report with review of the literature |
title_sort | cerebellar hemangioblastoma: case report with review of the literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8367806/ https://www.ncbi.nlm.nih.gov/pubmed/34429813 http://dx.doi.org/10.1016/j.radcr.2021.07.027 |
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