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Histone-mutant glioma presenting as diffuse leptomeningeal disease

Glioblastoma multiforme is the most common malignant primary brain tumor in adults. Histone H3 mutations have been identified in pediatric and adult gliomas, with H3K27M mutations typically associated with a posterior fossa midline tumor location and poor prognosis. Leptomeningeal disease is a known...

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Autores principales: Nadkarni, Tanvi, Hamilton, Kimberly, Niazi, Faraze, Ward, Melanie, Okakpu, Uchenna, Castellani, Rudolph J, Prisneac, Ion, Sener, Ugur
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Future Medicine Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8461753/
https://www.ncbi.nlm.nih.gov/pubmed/34469205
http://dx.doi.org/10.2217/cns-2021-0008
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author Nadkarni, Tanvi
Hamilton, Kimberly
Niazi, Faraze
Ward, Melanie
Okakpu, Uchenna
Castellani, Rudolph J
Prisneac, Ion
Sener, Ugur
author_facet Nadkarni, Tanvi
Hamilton, Kimberly
Niazi, Faraze
Ward, Melanie
Okakpu, Uchenna
Castellani, Rudolph J
Prisneac, Ion
Sener, Ugur
author_sort Nadkarni, Tanvi
collection PubMed
description Glioblastoma multiforme is the most common malignant primary brain tumor in adults. Histone H3 mutations have been identified in pediatric and adult gliomas, with H3K27M mutations typically associated with a posterior fossa midline tumor location and poor prognosis. Leptomeningeal disease is a known complication of histone-mutant glioma, but uncommon at the time of initial diagnosis. We describe a case of glioblastoma with H3K27M mutation that initially presented with progressive vision loss due to diffuse leptomeningeal disease in the absence of a mass lesion other than a small cerebellar area of enhancement and with cerebrospinal fluid cytology negative for malignant cells on two occasions, highlighting the importance of including primary CNS malignancies in the differential of diffuse radiographic leptomeningeal enhancement.
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spelling pubmed-84617532021-09-27 Histone-mutant glioma presenting as diffuse leptomeningeal disease Nadkarni, Tanvi Hamilton, Kimberly Niazi, Faraze Ward, Melanie Okakpu, Uchenna Castellani, Rudolph J Prisneac, Ion Sener, Ugur CNS Oncol Case Report Glioblastoma multiforme is the most common malignant primary brain tumor in adults. Histone H3 mutations have been identified in pediatric and adult gliomas, with H3K27M mutations typically associated with a posterior fossa midline tumor location and poor prognosis. Leptomeningeal disease is a known complication of histone-mutant glioma, but uncommon at the time of initial diagnosis. We describe a case of glioblastoma with H3K27M mutation that initially presented with progressive vision loss due to diffuse leptomeningeal disease in the absence of a mass lesion other than a small cerebellar area of enhancement and with cerebrospinal fluid cytology negative for malignant cells on two occasions, highlighting the importance of including primary CNS malignancies in the differential of diffuse radiographic leptomeningeal enhancement. Future Medicine Ltd 2021-09-01 /pmc/articles/PMC8461753/ /pubmed/34469205 http://dx.doi.org/10.2217/cns-2021-0008 Text en © 2021 Ugur Sener https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under the Attribution-NonCommercial-NoDerivatives 4.0 Unported License (https://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle Case Report
Nadkarni, Tanvi
Hamilton, Kimberly
Niazi, Faraze
Ward, Melanie
Okakpu, Uchenna
Castellani, Rudolph J
Prisneac, Ion
Sener, Ugur
Histone-mutant glioma presenting as diffuse leptomeningeal disease
title Histone-mutant glioma presenting as diffuse leptomeningeal disease
title_full Histone-mutant glioma presenting as diffuse leptomeningeal disease
title_fullStr Histone-mutant glioma presenting as diffuse leptomeningeal disease
title_full_unstemmed Histone-mutant glioma presenting as diffuse leptomeningeal disease
title_short Histone-mutant glioma presenting as diffuse leptomeningeal disease
title_sort histone-mutant glioma presenting as diffuse leptomeningeal disease
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8461753/
https://www.ncbi.nlm.nih.gov/pubmed/34469205
http://dx.doi.org/10.2217/cns-2021-0008
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