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Intradiploic Encephalocele at the Parietal Bone: A Case Report and Literature Review

Intradiploic encephalocele is a rare condition of herniation of the brain parenchyma through the diploic space. A 52-year-old man presented with a parietal intradiploic encephalocele manifesting as an intermittent headache for 7 months. CT revealed an osteolytic lesion involving the right parietal b...

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Autores principales: Jeong, Dong Jun, Lee, Boeun, Yang, Kookhee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Brain Tumor Society; The Korean Society for Neuro-Oncology; The Korean Society for Pediatric Neuro-Oncology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8819461/
https://www.ncbi.nlm.nih.gov/pubmed/35118847
http://dx.doi.org/10.14791/btrt.2022.10.e20
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author Jeong, Dong Jun
Lee, Boeun
Yang, Kookhee
author_facet Jeong, Dong Jun
Lee, Boeun
Yang, Kookhee
author_sort Jeong, Dong Jun
collection PubMed
description Intradiploic encephalocele is a rare condition of herniation of the brain parenchyma through the diploic space. A 52-year-old man presented with a parietal intradiploic encephalocele manifesting as an intermittent headache for 7 months. CT revealed an osteolytic lesion involving the right parietal bone. MRI demonstrated brain herniation within the diploic space. Surgery may be unnecessary in the absence of concurrent symptoms or neurological deficits. After 2 years of follow-up, symptoms were improved without neurological deficits and CT findings. We report the X-ray, CT, and MRI findings of an extremely rare case of parietal intradiploic encephalocele in adulthood.
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spelling pubmed-88194612022-02-15 Intradiploic Encephalocele at the Parietal Bone: A Case Report and Literature Review Jeong, Dong Jun Lee, Boeun Yang, Kookhee Brain Tumor Res Treat Case Report Intradiploic encephalocele is a rare condition of herniation of the brain parenchyma through the diploic space. A 52-year-old man presented with a parietal intradiploic encephalocele manifesting as an intermittent headache for 7 months. CT revealed an osteolytic lesion involving the right parietal bone. MRI demonstrated brain herniation within the diploic space. Surgery may be unnecessary in the absence of concurrent symptoms or neurological deficits. After 2 years of follow-up, symptoms were improved without neurological deficits and CT findings. We report the X-ray, CT, and MRI findings of an extremely rare case of parietal intradiploic encephalocele in adulthood. The Korean Brain Tumor Society; The Korean Society for Neuro-Oncology; The Korean Society for Pediatric Neuro-Oncology 2022-01 2022-01-17 /pmc/articles/PMC8819461/ /pubmed/35118847 http://dx.doi.org/10.14791/btrt.2022.10.e20 Text en Copyright © 2022 The Korean Brain Tumor Society, The Korean Society for Neuro-Oncology, and The Korean Society for Pediatric Neuro-Oncology https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Jeong, Dong Jun
Lee, Boeun
Yang, Kookhee
Intradiploic Encephalocele at the Parietal Bone: A Case Report and Literature Review
title Intradiploic Encephalocele at the Parietal Bone: A Case Report and Literature Review
title_full Intradiploic Encephalocele at the Parietal Bone: A Case Report and Literature Review
title_fullStr Intradiploic Encephalocele at the Parietal Bone: A Case Report and Literature Review
title_full_unstemmed Intradiploic Encephalocele at the Parietal Bone: A Case Report and Literature Review
title_short Intradiploic Encephalocele at the Parietal Bone: A Case Report and Literature Review
title_sort intradiploic encephalocele at the parietal bone: a case report and literature review
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8819461/
https://www.ncbi.nlm.nih.gov/pubmed/35118847
http://dx.doi.org/10.14791/btrt.2022.10.e20
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