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First Reported Case of Atypical Meningioma in an Individual with Down Syndrome
Individuals with Down syndrome are at decreased risk of developing most types of solid tumors, including central nervous system malignancies. Several mechanisms have been proposed to explain how additional genetic material on chromosome 21 may confer this increased protection. Only two individuals w...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
S. Karger AG
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9082194/ https://www.ncbi.nlm.nih.gov/pubmed/35611359 http://dx.doi.org/10.1159/000523665 |
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author | Vanderschelden, Rachel Golshani, Kiarash Evans, Mark G. |
author_facet | Vanderschelden, Rachel Golshani, Kiarash Evans, Mark G. |
author_sort | Vanderschelden, Rachel |
collection | PubMed |
description | Individuals with Down syndrome are at decreased risk of developing most types of solid tumors, including central nervous system malignancies. Several mechanisms have been proposed to explain how additional genetic material on chromosome 21 may confer this increased protection. Only two individuals with Down syndrome and meningioma have been described in the medical literature, whose tumors were both World Health Organization (WHO) grade 1. Here, we report the first individual with Down syndrome to our knowledge who developed an atypical meningioma, WHO grade 2. We also provide a hypothesis for how this tumor could have arisen in the setting of trisomy 21. |
format | Online Article Text |
id | pubmed-9082194 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | S. Karger AG |
record_format | MEDLINE/PubMed |
spelling | pubmed-90821942022-05-23 First Reported Case of Atypical Meningioma in an Individual with Down Syndrome Vanderschelden, Rachel Golshani, Kiarash Evans, Mark G. Case Rep Neurol Single Case − General Neurology Individuals with Down syndrome are at decreased risk of developing most types of solid tumors, including central nervous system malignancies. Several mechanisms have been proposed to explain how additional genetic material on chromosome 21 may confer this increased protection. Only two individuals with Down syndrome and meningioma have been described in the medical literature, whose tumors were both World Health Organization (WHO) grade 1. Here, we report the first individual with Down syndrome to our knowledge who developed an atypical meningioma, WHO grade 2. We also provide a hypothesis for how this tumor could have arisen in the setting of trisomy 21. S. Karger AG 2022-04-04 /pmc/articles/PMC9082194/ /pubmed/35611359 http://dx.doi.org/10.1159/000523665 Text en Copyright © 2022 by S. Karger AG, Basel https://creativecommons.org/licenses/by-nc/4.0/This article is licensed under the Creative Commons Attribution-NonCommercial-4.0 International License (CC BY-NC) (http://www.karger.com/Services/OpenAccessLicense). Usage and distribution for commercial purposes requires written permission. |
spellingShingle | Single Case − General Neurology Vanderschelden, Rachel Golshani, Kiarash Evans, Mark G. First Reported Case of Atypical Meningioma in an Individual with Down Syndrome |
title | First Reported Case of Atypical Meningioma in an Individual with Down Syndrome |
title_full | First Reported Case of Atypical Meningioma in an Individual with Down Syndrome |
title_fullStr | First Reported Case of Atypical Meningioma in an Individual with Down Syndrome |
title_full_unstemmed | First Reported Case of Atypical Meningioma in an Individual with Down Syndrome |
title_short | First Reported Case of Atypical Meningioma in an Individual with Down Syndrome |
title_sort | first reported case of atypical meningioma in an individual with down syndrome |
topic | Single Case − General Neurology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9082194/ https://www.ncbi.nlm.nih.gov/pubmed/35611359 http://dx.doi.org/10.1159/000523665 |
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