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A case of idiopathic encephalomeningocele

In the present case we report about an encephalomeningocele in an adult female. Since the cause of this medical entity is a congenital fusion defect of the neural tube of the cranial base, most of the encephaloceles occurs in children leading to facial disfigurement. In the rare cases described in a...

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Autores principales: Petridis, Athanasios K., Doukas, Alexandros, Mehdorn, Hubertus M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PAGEPress Publications 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3981251/
https://www.ncbi.nlm.nih.gov/pubmed/24765291
http://dx.doi.org/10.4081/cp.2011.e29
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author Petridis, Athanasios K.
Doukas, Alexandros
Mehdorn, Hubertus M.
author_facet Petridis, Athanasios K.
Doukas, Alexandros
Mehdorn, Hubertus M.
author_sort Petridis, Athanasios K.
collection PubMed
description In the present case we report about an encephalomeningocele in an adult female. Since the cause of this medical entity is a congenital fusion defect of the neural tube of the cranial base, most of the encephaloceles occurs in children leading to facial disfigurement. In the rare cases described in adults, rhinorrhea is usually present. Here we present a case of temporobasal encephalomeningocele in a 72-year-old female patient suffering from headaches in the last 4–5 years. No rhinorrhea or other significant neurological symptoms were noticed. No congenital cause was apparent. After diagnostic steps including brain magnetic resonance imaging (MRI), cranial computed tomography (CT) and MR cisternography, an encephalomeningocele was diagnosed. Through a pterional approach this was completely removed. The only symptom the patient complaint about, headache, was eliminated after surgery.
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spelling pubmed-39812512014-04-24 A case of idiopathic encephalomeningocele Petridis, Athanasios K. Doukas, Alexandros Mehdorn, Hubertus M. Clin Pract Article In the present case we report about an encephalomeningocele in an adult female. Since the cause of this medical entity is a congenital fusion defect of the neural tube of the cranial base, most of the encephaloceles occurs in children leading to facial disfigurement. In the rare cases described in adults, rhinorrhea is usually present. Here we present a case of temporobasal encephalomeningocele in a 72-year-old female patient suffering from headaches in the last 4–5 years. No rhinorrhea or other significant neurological symptoms were noticed. No congenital cause was apparent. After diagnostic steps including brain magnetic resonance imaging (MRI), cranial computed tomography (CT) and MR cisternography, an encephalomeningocele was diagnosed. Through a pterional approach this was completely removed. The only symptom the patient complaint about, headache, was eliminated after surgery. PAGEPress Publications 2011-05-06 /pmc/articles/PMC3981251/ /pubmed/24765291 http://dx.doi.org/10.4081/cp.2011.e29 Text en ©Copyright A.K. Petridis et al., 2011 This work is licensed under a Creative Commons Attribution 3.0 License (by-nc 3.0). Licensee PAGEPress, Italy
spellingShingle Article
Petridis, Athanasios K.
Doukas, Alexandros
Mehdorn, Hubertus M.
A case of idiopathic encephalomeningocele
title A case of idiopathic encephalomeningocele
title_full A case of idiopathic encephalomeningocele
title_fullStr A case of idiopathic encephalomeningocele
title_full_unstemmed A case of idiopathic encephalomeningocele
title_short A case of idiopathic encephalomeningocele
title_sort case of idiopathic encephalomeningocele
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3981251/
https://www.ncbi.nlm.nih.gov/pubmed/24765291
http://dx.doi.org/10.4081/cp.2011.e29
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