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Intramedullary sclerosing meningioma: operative video
Sclerosing meningiomas (SMs) represent a rare histological variant of meningiomas, first described in 1989 as invasive bulking masses of whorling collagen bundles with a minimum percentage of meningothelia-resembling cells, and they are often misdiagnosed. The literature reports only 30 cases of SMs...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association of Neurological Surgeons
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10581006/ https://www.ncbi.nlm.nih.gov/pubmed/37854649 http://dx.doi.org/10.3171/2023.7.FOCVID2385 |
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author | Garufi, Giada Ricciardo, Giuseppe Conti, Alfredo Cardali, Salvatore Massimiliano |
author_facet | Garufi, Giada Ricciardo, Giuseppe Conti, Alfredo Cardali, Salvatore Massimiliano |
author_sort | Garufi, Giada |
collection | PubMed |
description | Sclerosing meningiomas (SMs) represent a rare histological variant of meningiomas, first described in 1989 as invasive bulking masses of whorling collagen bundles with a minimum percentage of meningothelia-resembling cells, and they are often misdiagnosed. The literature reports only 30 cases of SMs, with only two of them being intramedullary. The authors present the case of a patient with a cervical intramedullary SM who presented with gait disturbances, sensory deficits, weakness in four extremities, and hyperreflexia. The surgery was performed under neurophysiological monitoring and after administration of sodium fluorescein, which allowed us to discriminate the exact myelotomy point. Intramedullary SMs are very rare entities whose correct management may result in a good outcome. |
format | Online Article Text |
id | pubmed-10581006 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Association of Neurological Surgeons |
record_format | MEDLINE/PubMed |
spelling | pubmed-105810062023-10-18 Intramedullary sclerosing meningioma: operative video Garufi, Giada Ricciardo, Giuseppe Conti, Alfredo Cardali, Salvatore Massimiliano Neurosurg Focus Video Article Sclerosing meningiomas (SMs) represent a rare histological variant of meningiomas, first described in 1989 as invasive bulking masses of whorling collagen bundles with a minimum percentage of meningothelia-resembling cells, and they are often misdiagnosed. The literature reports only 30 cases of SMs, with only two of them being intramedullary. The authors present the case of a patient with a cervical intramedullary SM who presented with gait disturbances, sensory deficits, weakness in four extremities, and hyperreflexia. The surgery was performed under neurophysiological monitoring and after administration of sodium fluorescein, which allowed us to discriminate the exact myelotomy point. Intramedullary SMs are very rare entities whose correct management may result in a good outcome. American Association of Neurological Surgeons 2023-10-01 /pmc/articles/PMC10581006/ /pubmed/37854649 http://dx.doi.org/10.3171/2023.7.FOCVID2385 Text en © 2023, The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the CC BY license (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ). |
spellingShingle | Article Garufi, Giada Ricciardo, Giuseppe Conti, Alfredo Cardali, Salvatore Massimiliano Intramedullary sclerosing meningioma: operative video |
title | Intramedullary sclerosing meningioma: operative video |
title_full | Intramedullary sclerosing meningioma: operative video |
title_fullStr | Intramedullary sclerosing meningioma: operative video |
title_full_unstemmed | Intramedullary sclerosing meningioma: operative video |
title_short | Intramedullary sclerosing meningioma: operative video |
title_sort | intramedullary sclerosing meningioma: operative video |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10581006/ https://www.ncbi.nlm.nih.gov/pubmed/37854649 http://dx.doi.org/10.3171/2023.7.FOCVID2385 |
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