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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...

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Autores principales: Okonkwo, Sunday Nnamdi, Afghani, Tayyab, Akbar, Maheen, Manzoor, Amna, Asif, Muhammad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
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.
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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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