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Diffuse midline glioma in Ollier disease: A case report and a brief review of the literature
Ollier disease is a rare condition presenting with enchondromas in an irregular distribution within the medullary cavity of bones. The disease is well known for sarcomatous transformation to chondrosarcomas. It also increases the risk of other malignancies like leukemia, ovarian tumors, and glial tu...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8237312/ https://www.ncbi.nlm.nih.gov/pubmed/34194594 http://dx.doi.org/10.1016/j.radcr.2021.05.046 |
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author | Karabulut, Ahmet Kasım Türk, Sevcan Tamsel, İpek Kim, John Argın, Mehmet |
author_facet | Karabulut, Ahmet Kasım Türk, Sevcan Tamsel, İpek Kim, John Argın, Mehmet |
author_sort | Karabulut, Ahmet Kasım |
collection | PubMed |
description | Ollier disease is a rare condition presenting with enchondromas in an irregular distribution within the medullary cavity of bones. The disease is well known for sarcomatous transformation to chondrosarcomas. It also increases the risk of other malignancies like leukemia, ovarian tumors, and glial tumors. Central nervous system malignancies associated with Ollier disease are thought to arise by somatic IDH mosaicism with their atypical features of distribution, multifocality, and age of onset. We present a case with imaging consistent with diffuse midline glioma in a patient with Ollier disease. We conclude with a brief review of the literature on Ollier Disease with a focus on central nervous system malignancies, tumorigenesis and pathophysiology. |
format | Online Article Text |
id | pubmed-8237312 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-82373122021-06-29 Diffuse midline glioma in Ollier disease: A case report and a brief review of the literature Karabulut, Ahmet Kasım Türk, Sevcan Tamsel, İpek Kim, John Argın, Mehmet Radiol Case Rep Case Report Ollier disease is a rare condition presenting with enchondromas in an irregular distribution within the medullary cavity of bones. The disease is well known for sarcomatous transformation to chondrosarcomas. It also increases the risk of other malignancies like leukemia, ovarian tumors, and glial tumors. Central nervous system malignancies associated with Ollier disease are thought to arise by somatic IDH mosaicism with their atypical features of distribution, multifocality, and age of onset. We present a case with imaging consistent with diffuse midline glioma in a patient with Ollier disease. We conclude with a brief review of the literature on Ollier Disease with a focus on central nervous system malignancies, tumorigenesis and pathophysiology. Elsevier 2021-06-20 /pmc/articles/PMC8237312/ /pubmed/34194594 http://dx.doi.org/10.1016/j.radcr.2021.05.046 Text en © 2021 The Authors. Published by Elsevier Inc. on behalf of University of Washington. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Case Report Karabulut, Ahmet Kasım Türk, Sevcan Tamsel, İpek Kim, John Argın, Mehmet Diffuse midline glioma in Ollier disease: A case report and a brief review of the literature |
title | Diffuse midline glioma in Ollier disease: A case report and a brief review of the literature |
title_full | Diffuse midline glioma in Ollier disease: A case report and a brief review of the literature |
title_fullStr | Diffuse midline glioma in Ollier disease: A case report and a brief review of the literature |
title_full_unstemmed | Diffuse midline glioma in Ollier disease: A case report and a brief review of the literature |
title_short | Diffuse midline glioma in Ollier disease: A case report and a brief review of the literature |
title_sort | diffuse midline glioma in ollier disease: a case report and a brief review of the literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8237312/ https://www.ncbi.nlm.nih.gov/pubmed/34194594 http://dx.doi.org/10.1016/j.radcr.2021.05.046 |
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