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The role of methylation profiling in histologically diagnosed neurocytoma: a case series

PURPOSE: To highlight the clinical, neuroradiographic, neuropathologic, and molecular features of histologically identified neurocytoma in a pediatric cohort and highlight the evolving use methylation profiling in providing diagnostic clarity in difficult to diagnosis pediatric brain tumors. METHODS...

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Autores principales: Kalawi, Adam Z., Malicki, Denise M., Abdullaev, Zied, Pratt, Drew W., Quezado, Martha, Aldape, Kenneth, Elster, Jennifer D., Paul, Megan R., Khanna, Paritosh C., Levy, Michael L., Crawford, John R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9477906/
https://www.ncbi.nlm.nih.gov/pubmed/35994156
http://dx.doi.org/10.1007/s11060-022-04117-1
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author Kalawi, Adam Z.
Malicki, Denise M.
Abdullaev, Zied
Pratt, Drew W.
Quezado, Martha
Aldape, Kenneth
Elster, Jennifer D.
Paul, Megan R.
Khanna, Paritosh C.
Levy, Michael L.
Crawford, John R.
author_facet Kalawi, Adam Z.
Malicki, Denise M.
Abdullaev, Zied
Pratt, Drew W.
Quezado, Martha
Aldape, Kenneth
Elster, Jennifer D.
Paul, Megan R.
Khanna, Paritosh C.
Levy, Michael L.
Crawford, John R.
author_sort Kalawi, Adam Z.
collection PubMed
description PURPOSE: To highlight the clinical, neuroradiographic, neuropathologic, and molecular features of histologically identified neurocytoma in a pediatric cohort and highlight the evolving use methylation profiling in providing diagnostic clarity in difficult to diagnosis pediatric brain tumors. METHODS: Five consecutive children (ages 9–13, 2 girls 3 boys) were histologically diagnosed with neurocytoma at Rady Children’s Hospital San Diego from 2012 to 2018. Clinical and molecular features were analyzed with regards to treatment course and outcome. RESULTS: Presenting symptoms included seizures (n = 2), syncope (n = 1), headache (n = 2), visual disturbances (n = 2) and emesis (n = 2). Tumor location included intraventricular (n = 2), intraventricular with parenchymal spread (n = 1), and extraventricular (n = 2). Magnetic resonance imaging demonstrated reduced diffusivity (2/5), signal abnormality on susceptibility-weighted sequences (3/5), and varying degrees of contrast enhancement (4/5). All patients underwent surgical resection alone. Recurrence occurred in four children that were treated with surgery (4/4), adjuvant radiation (2/4), and chemoradiation (1/4). Neuropathologic features included positivity for GFAP (4/5), synaptophysin (4/5), NSE (2/2), NeuN (4/4), and variable Ki-67 (< 1% to 15%). Next generation sequencing (3/5) and microarray (3/5) collectively were abnormal in four of five tumors. Methylation profiling was successfully performed on four of five samples which led to modification of diagnosis in two patients and the others were either unclassifiable or confirmatory with the histologic diagnosis. Mean time to follow up was 77 months (range 44–112 months). Mean progression free survival and overall survival were 24 months (range 6 to 52 months) and 100% respectively. CONCLUSION: Neurocytomas are a rare clinical entity that warrants further investigation into molecular and pathologic prognosticating features. Methylation profiling may aid in differentiation of neurocytoma from other difficult to diagnose tumors who share similar histologic features.
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spelling pubmed-94779062022-09-17 The role of methylation profiling in histologically diagnosed neurocytoma: a case series Kalawi, Adam Z. Malicki, Denise M. Abdullaev, Zied Pratt, Drew W. Quezado, Martha Aldape, Kenneth Elster, Jennifer D. Paul, Megan R. Khanna, Paritosh C. Levy, Michael L. Crawford, John R. J Neurooncol Research PURPOSE: To highlight the clinical, neuroradiographic, neuropathologic, and molecular features of histologically identified neurocytoma in a pediatric cohort and highlight the evolving use methylation profiling in providing diagnostic clarity in difficult to diagnosis pediatric brain tumors. METHODS: Five consecutive children (ages 9–13, 2 girls 3 boys) were histologically diagnosed with neurocytoma at Rady Children’s Hospital San Diego from 2012 to 2018. Clinical and molecular features were analyzed with regards to treatment course and outcome. RESULTS: Presenting symptoms included seizures (n = 2), syncope (n = 1), headache (n = 2), visual disturbances (n = 2) and emesis (n = 2). Tumor location included intraventricular (n = 2), intraventricular with parenchymal spread (n = 1), and extraventricular (n = 2). Magnetic resonance imaging demonstrated reduced diffusivity (2/5), signal abnormality on susceptibility-weighted sequences (3/5), and varying degrees of contrast enhancement (4/5). All patients underwent surgical resection alone. Recurrence occurred in four children that were treated with surgery (4/4), adjuvant radiation (2/4), and chemoradiation (1/4). Neuropathologic features included positivity for GFAP (4/5), synaptophysin (4/5), NSE (2/2), NeuN (4/4), and variable Ki-67 (< 1% to 15%). Next generation sequencing (3/5) and microarray (3/5) collectively were abnormal in four of five tumors. Methylation profiling was successfully performed on four of five samples which led to modification of diagnosis in two patients and the others were either unclassifiable or confirmatory with the histologic diagnosis. Mean time to follow up was 77 months (range 44–112 months). Mean progression free survival and overall survival were 24 months (range 6 to 52 months) and 100% respectively. CONCLUSION: Neurocytomas are a rare clinical entity that warrants further investigation into molecular and pathologic prognosticating features. Methylation profiling may aid in differentiation of neurocytoma from other difficult to diagnose tumors who share similar histologic features. Springer US 2022-08-22 2022 /pmc/articles/PMC9477906/ /pubmed/35994156 http://dx.doi.org/10.1007/s11060-022-04117-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research
Kalawi, Adam Z.
Malicki, Denise M.
Abdullaev, Zied
Pratt, Drew W.
Quezado, Martha
Aldape, Kenneth
Elster, Jennifer D.
Paul, Megan R.
Khanna, Paritosh C.
Levy, Michael L.
Crawford, John R.
The role of methylation profiling in histologically diagnosed neurocytoma: a case series
title The role of methylation profiling in histologically diagnosed neurocytoma: a case series
title_full The role of methylation profiling in histologically diagnosed neurocytoma: a case series
title_fullStr The role of methylation profiling in histologically diagnosed neurocytoma: a case series
title_full_unstemmed The role of methylation profiling in histologically diagnosed neurocytoma: a case series
title_short The role of methylation profiling in histologically diagnosed neurocytoma: a case series
title_sort role of methylation profiling in histologically diagnosed neurocytoma: a case series
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9477906/
https://www.ncbi.nlm.nih.gov/pubmed/35994156
http://dx.doi.org/10.1007/s11060-022-04117-1
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