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The application of fluorescence techniques in meningioma surgery—a review

Surgical resections of meningiomas, the most common intracranial tumor in adults, can only be curative if radical resection is achieved. Potentially, the extent of resection could be improved, especially in complex and/or high-grade meningiomas by fluorescence-guided surgery using 5-aminolevulinic a...

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Autores principales: Dijkstra, Bianca M., Jeltema, Hanne-Rinck (J.R.), Kruijff, Schelto, Groen, Rob J. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6821664/
https://www.ncbi.nlm.nih.gov/pubmed/30519770
http://dx.doi.org/10.1007/s10143-018-01062-4
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author Dijkstra, Bianca M.
Jeltema, Hanne-Rinck (J.R.)
Kruijff, Schelto
Groen, Rob J. M.
author_facet Dijkstra, Bianca M.
Jeltema, Hanne-Rinck (J.R.)
Kruijff, Schelto
Groen, Rob J. M.
author_sort Dijkstra, Bianca M.
collection PubMed
description Surgical resections of meningiomas, the most common intracranial tumor in adults, can only be curative if radical resection is achieved. Potentially, the extent of resection could be improved, especially in complex and/or high-grade meningiomas by fluorescence-guided surgery using 5-aminolevulinic acid (5-ALA), indocyanine green (ICG), or fluorescein. This review aims to summarize and evaluate these fluorescence-guided meningioma surgery techniques. PubMed and Embase were searched for relevant articles. Additionally, we checked reference lists for further studies. Forty-eight articles were included in the final analysis. 5-ALA fluoresced with varying sensitivity and selectivity in meningiomas and in invaded bone and dura mater. Although ICG was mainly applied for video angiography, one report shows tumor fluorescence 18–28 h post-ICG injection. Lastly, the use of fluorescein could aid in the identification of tumor remnants; however, detection of dural tail is highly questionable. Fluorescence-guided meningioma surgery should be a reliable, highly specific, and sensitive technique. Despite numerous studies reporting the use of fluorescent dyes, currently, there is no evidence that these tools improve the radical resection rate and long-term recurrence-free outcome in meningioma surgery without neurological deficits. Evidence regarding the effectiveness and increased safety of resection after the application of these fluorophores is currently lacking. Future research should focus on the development of a meningioma-targeted, highly sensitive, and specific fluorophore. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10143-018-01062-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-68216642019-11-06 The application of fluorescence techniques in meningioma surgery—a review Dijkstra, Bianca M. Jeltema, Hanne-Rinck (J.R.) Kruijff, Schelto Groen, Rob J. M. Neurosurg Rev Review Surgical resections of meningiomas, the most common intracranial tumor in adults, can only be curative if radical resection is achieved. Potentially, the extent of resection could be improved, especially in complex and/or high-grade meningiomas by fluorescence-guided surgery using 5-aminolevulinic acid (5-ALA), indocyanine green (ICG), or fluorescein. This review aims to summarize and evaluate these fluorescence-guided meningioma surgery techniques. PubMed and Embase were searched for relevant articles. Additionally, we checked reference lists for further studies. Forty-eight articles were included in the final analysis. 5-ALA fluoresced with varying sensitivity and selectivity in meningiomas and in invaded bone and dura mater. Although ICG was mainly applied for video angiography, one report shows tumor fluorescence 18–28 h post-ICG injection. Lastly, the use of fluorescein could aid in the identification of tumor remnants; however, detection of dural tail is highly questionable. Fluorescence-guided meningioma surgery should be a reliable, highly specific, and sensitive technique. Despite numerous studies reporting the use of fluorescent dyes, currently, there is no evidence that these tools improve the radical resection rate and long-term recurrence-free outcome in meningioma surgery without neurological deficits. Evidence regarding the effectiveness and increased safety of resection after the application of these fluorophores is currently lacking. Future research should focus on the development of a meningioma-targeted, highly sensitive, and specific fluorophore. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10143-018-01062-4) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2018-12-06 2019 /pmc/articles/PMC6821664/ /pubmed/30519770 http://dx.doi.org/10.1007/s10143-018-01062-4 Text en © The Author(s) 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Review
Dijkstra, Bianca M.
Jeltema, Hanne-Rinck (J.R.)
Kruijff, Schelto
Groen, Rob J. M.
The application of fluorescence techniques in meningioma surgery—a review
title The application of fluorescence techniques in meningioma surgery—a review
title_full The application of fluorescence techniques in meningioma surgery—a review
title_fullStr The application of fluorescence techniques in meningioma surgery—a review
title_full_unstemmed The application of fluorescence techniques in meningioma surgery—a review
title_short The application of fluorescence techniques in meningioma surgery—a review
title_sort application of fluorescence techniques in meningioma surgery—a review
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6821664/
https://www.ncbi.nlm.nih.gov/pubmed/30519770
http://dx.doi.org/10.1007/s10143-018-01062-4
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