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A Rare Case of Sphenoid Encephalocoele Presenting with Fifth Cranial Nerve Involvement

A 14-year-old girl presented with chronic headache, recurrent episodes of vomiting, fever, and two episodes of generalized tonic clonic seizure in the past 2 months. Neuroimaging revealed herniation of the brain along with the dura through a defect in the left greater wing of the sphenoid. Left pter...

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Autores principales: Wadikhaye, Rohit, Yerramneni, Vamsi Krishna, Yerragunta, Thirumal, Sharma, Neeraj
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7227746/
https://www.ncbi.nlm.nih.gov/pubmed/32435302
http://dx.doi.org/10.4103/JPN.JPN_8_19
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author Wadikhaye, Rohit
Yerramneni, Vamsi Krishna
Yerragunta, Thirumal
Sharma, Neeraj
author_facet Wadikhaye, Rohit
Yerramneni, Vamsi Krishna
Yerragunta, Thirumal
Sharma, Neeraj
author_sort Wadikhaye, Rohit
collection PubMed
description A 14-year-old girl presented with chronic headache, recurrent episodes of vomiting, fever, and two episodes of generalized tonic clonic seizure in the past 2 months. Neuroimaging revealed herniation of the brain along with the dura through a defect in the left greater wing of the sphenoid. Left pterional craniotomy was carried out. Herniation of the dural sac along with its contents through the bony defect in the greater sphenoid wing was identified lateral to the V2 nerve passing through the foramen rotundum. The dural defect was repaired. Bony defect was covered with a circular titanium plate. The patient did not have cerebrospinal fluid rhinorrhea postoperatively. At 6-month follow-up, she was asymptomatic.
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spelling pubmed-72277462020-05-20 A Rare Case of Sphenoid Encephalocoele Presenting with Fifth Cranial Nerve Involvement Wadikhaye, Rohit Yerramneni, Vamsi Krishna Yerragunta, Thirumal Sharma, Neeraj J Pediatr Neurosci Case Report A 14-year-old girl presented with chronic headache, recurrent episodes of vomiting, fever, and two episodes of generalized tonic clonic seizure in the past 2 months. Neuroimaging revealed herniation of the brain along with the dura through a defect in the left greater wing of the sphenoid. Left pterional craniotomy was carried out. Herniation of the dural sac along with its contents through the bony defect in the greater sphenoid wing was identified lateral to the V2 nerve passing through the foramen rotundum. The dural defect was repaired. Bony defect was covered with a circular titanium plate. The patient did not have cerebrospinal fluid rhinorrhea postoperatively. At 6-month follow-up, she was asymptomatic. Wolters Kluwer - Medknow 2020 2020-03-18 /pmc/articles/PMC7227746/ /pubmed/32435302 http://dx.doi.org/10.4103/JPN.JPN_8_19 Text en Copyright: © 2020 Journal of Pediatric Neurosciences 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
Wadikhaye, Rohit
Yerramneni, Vamsi Krishna
Yerragunta, Thirumal
Sharma, Neeraj
A Rare Case of Sphenoid Encephalocoele Presenting with Fifth Cranial Nerve Involvement
title A Rare Case of Sphenoid Encephalocoele Presenting with Fifth Cranial Nerve Involvement
title_full A Rare Case of Sphenoid Encephalocoele Presenting with Fifth Cranial Nerve Involvement
title_fullStr A Rare Case of Sphenoid Encephalocoele Presenting with Fifth Cranial Nerve Involvement
title_full_unstemmed A Rare Case of Sphenoid Encephalocoele Presenting with Fifth Cranial Nerve Involvement
title_short A Rare Case of Sphenoid Encephalocoele Presenting with Fifth Cranial Nerve Involvement
title_sort rare case of sphenoid encephalocoele presenting with fifth cranial nerve involvement
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7227746/
https://www.ncbi.nlm.nih.gov/pubmed/32435302
http://dx.doi.org/10.4103/JPN.JPN_8_19
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