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Multimodal neuroimaging of gliomatosis cerebri: a case series of four patients

In the latest World Health Organization classification of brain tumors, gliomatosis cerebri has been redefined to varying subsets of diffuse gliomas; however, the term is still used to describe gliomas with infiltrative growth into three or more cerebral lobes. These tumors are frequently misdiagnos...

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Autores principales: Bonomi, Robin, John, Flora, Patel, Suketu, Barger, Geoffery, Robinette, Natasha, Amit-Yousif, Alit J, Dominello, Michael, Juhasz, Csaba
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7444143/
https://www.ncbi.nlm.nih.gov/pubmed/32913666
http://dx.doi.org/10.1177/2058460120942789
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author Bonomi, Robin
John, Flora
Patel, Suketu
Barger, Geoffery
Robinette, Natasha
Amit-Yousif, Alit J
Dominello, Michael
Juhasz, Csaba
author_facet Bonomi, Robin
John, Flora
Patel, Suketu
Barger, Geoffery
Robinette, Natasha
Amit-Yousif, Alit J
Dominello, Michael
Juhasz, Csaba
author_sort Bonomi, Robin
collection PubMed
description In the latest World Health Organization classification of brain tumors, gliomatosis cerebri has been redefined to varying subsets of diffuse gliomas; however, the term is still used to describe gliomas with infiltrative growth into three or more cerebral lobes. These tumors are frequently misdiagnosed and difficult to treat due to their atypical presentation using structural imaging modalities including computed tomography and T1/T2-weighted magnetic resonance imaging (MRI). In this retrospective case series, we compared clinical MRI to amino acid positron emission tomography (PET) to assess the potential value of PET in the assessment of the extent of tumor involvement and in monitoring disease progression. We report the clinical course and serial multimodal imaging findings of four patients. Each patient presented at varying points in disease progression with widespread glioma brain involvement and was evaluated at least once by amino acid PET using alpha-[(11)C]methyl-L-tryptophan ([(11)C]-AMT). Increased uptake of [(11)C]-AMT was detected in a subset of non-enhancing brain lesions and detected tumor invasion before MRI signs of tumor in some regions. Increased uptake of [(11)C]-AMT was also detected in tumorous regions not detected by perfusion MRI or MR spectroscopy. Metabolic response to treatment was also observed in two patients. Overall, these data are consistent with and expand upon previous reports using other amino acid PET tracers in gliomatosis and show the potential added value of this imaging modality to clinical MRI in the detection and monitoring of these diffusely infiltrative tumors.
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spelling pubmed-74441432020-09-09 Multimodal neuroimaging of gliomatosis cerebri: a case series of four patients Bonomi, Robin John, Flora Patel, Suketu Barger, Geoffery Robinette, Natasha Amit-Yousif, Alit J Dominello, Michael Juhasz, Csaba Acta Radiol Open Case Report In the latest World Health Organization classification of brain tumors, gliomatosis cerebri has been redefined to varying subsets of diffuse gliomas; however, the term is still used to describe gliomas with infiltrative growth into three or more cerebral lobes. These tumors are frequently misdiagnosed and difficult to treat due to their atypical presentation using structural imaging modalities including computed tomography and T1/T2-weighted magnetic resonance imaging (MRI). In this retrospective case series, we compared clinical MRI to amino acid positron emission tomography (PET) to assess the potential value of PET in the assessment of the extent of tumor involvement and in monitoring disease progression. We report the clinical course and serial multimodal imaging findings of four patients. Each patient presented at varying points in disease progression with widespread glioma brain involvement and was evaluated at least once by amino acid PET using alpha-[(11)C]methyl-L-tryptophan ([(11)C]-AMT). Increased uptake of [(11)C]-AMT was detected in a subset of non-enhancing brain lesions and detected tumor invasion before MRI signs of tumor in some regions. Increased uptake of [(11)C]-AMT was also detected in tumorous regions not detected by perfusion MRI or MR spectroscopy. Metabolic response to treatment was also observed in two patients. Overall, these data are consistent with and expand upon previous reports using other amino acid PET tracers in gliomatosis and show the potential added value of this imaging modality to clinical MRI in the detection and monitoring of these diffusely infiltrative tumors. SAGE Publications 2020-08-21 /pmc/articles/PMC7444143/ /pubmed/32913666 http://dx.doi.org/10.1177/2058460120942789 Text en © The Foundation Acta Radiologica 2020 https://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Case Report
Bonomi, Robin
John, Flora
Patel, Suketu
Barger, Geoffery
Robinette, Natasha
Amit-Yousif, Alit J
Dominello, Michael
Juhasz, Csaba
Multimodal neuroimaging of gliomatosis cerebri: a case series of four patients
title Multimodal neuroimaging of gliomatosis cerebri: a case series of four patients
title_full Multimodal neuroimaging of gliomatosis cerebri: a case series of four patients
title_fullStr Multimodal neuroimaging of gliomatosis cerebri: a case series of four patients
title_full_unstemmed Multimodal neuroimaging of gliomatosis cerebri: a case series of four patients
title_short Multimodal neuroimaging of gliomatosis cerebri: a case series of four patients
title_sort multimodal neuroimaging of gliomatosis cerebri: a case series of four patients
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7444143/
https://www.ncbi.nlm.nih.gov/pubmed/32913666
http://dx.doi.org/10.1177/2058460120942789
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