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A case of idiopathic encephalomeningocele

Authors :
Athanasios K. Petridis
Alexandros Doukas
Hubertus M. Mehdorn
Source :
Clinics and Practice, Vol 1, Iss 2 (2011)
Publication Year :
2011
Publisher :
MDPI AG, 2011.

Abstract

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.

Details

Language :
English
ISSN :
20397275 and 20397283
Volume :
1
Issue :
2
Database :
Directory of Open Access Journals
Journal :
Clinics and Practice
Publication Type :
Academic Journal
Accession number :
edsdoj.754113e61b6b43d9b9026de1799e69cf
Document Type :
article
Full Text :
https://doi.org/10.4081/cp.2011.e29