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Bilateral orbital glial heterotopia: A rare case report
Glial heterotopia is a rare congenital mass that often presents as a unilateral mass lesion in or around the nose. Complete surgical excision is the treatment of choice. However, before any surgical intervention for suspected glial heterotopia, distinction should be made both clinically and radiolog...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6219331/ https://www.ncbi.nlm.nih.gov/pubmed/30505127 http://dx.doi.org/10.4103/ojo.OJO_214_2017 |
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author | Okonkwo, Sunday Nnamdi Afghani, Tayyab Akbar, Maheen Manzoor, Amna Asif, Muhammad |
author_facet | Okonkwo, Sunday Nnamdi Afghani, Tayyab Akbar, Maheen Manzoor, Amna Asif, Muhammad |
author_sort | Okonkwo, Sunday Nnamdi |
collection | PubMed |
description | Glial heterotopia is a rare congenital mass that often presents as a unilateral mass lesion in or around the nose. Complete surgical excision is the treatment of choice. However, before any surgical intervention for suspected glial heterotopia, distinction should be made both clinically and radiologically from the pathologically related encephalocele to prevent the risk of cerebrospinal fluid leak and meningitis. Here, we report a rare case of bilateral orbital glial heterotopia in a 2-year-old child with review of the literature. |
format | Online Article Text |
id | pubmed-6219331 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-62193312018-11-30 Bilateral orbital glial heterotopia: A rare case report Okonkwo, Sunday Nnamdi Afghani, Tayyab Akbar, Maheen Manzoor, Amna Asif, Muhammad Oman J Ophthalmol Case Report Glial heterotopia is a rare congenital mass that often presents as a unilateral mass lesion in or around the nose. Complete surgical excision is the treatment of choice. However, before any surgical intervention for suspected glial heterotopia, distinction should be made both clinically and radiologically from the pathologically related encephalocele to prevent the risk of cerebrospinal fluid leak and meningitis. Here, we report a rare case of bilateral orbital glial heterotopia in a 2-year-old child with review of the literature. Medknow Publications & Media Pvt Ltd 2018 /pmc/articles/PMC6219331/ /pubmed/30505127 http://dx.doi.org/10.4103/ojo.OJO_214_2017 Text en Copyright: © 2018 Oman Ophthalmic Society http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Case Report Okonkwo, Sunday Nnamdi Afghani, Tayyab Akbar, Maheen Manzoor, Amna Asif, Muhammad Bilateral orbital glial heterotopia: A rare case report |
title | Bilateral orbital glial heterotopia: A rare case report |
title_full | Bilateral orbital glial heterotopia: A rare case report |
title_fullStr | Bilateral orbital glial heterotopia: A rare case report |
title_full_unstemmed | Bilateral orbital glial heterotopia: A rare case report |
title_short | Bilateral orbital glial heterotopia: A rare case report |
title_sort | bilateral orbital glial heterotopia: a rare case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6219331/ https://www.ncbi.nlm.nih.gov/pubmed/30505127 http://dx.doi.org/10.4103/ojo.OJO_214_2017 |
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