A case of idiopathic encephalomeningocele

  • Athanasios K. Petridis Department of Neurosurgery, University Hospital of Schleswig-Holstein, Campus Kiel, Germany.
  • Alexandros Doukas | opticdisc@aol.com Department of Neurosurgery, University Hospital of Schleswig-Holstein, Campus Kiel, Germany.
  • Hubertus M. Mehdorn Department of Neurosurgery, University Hospital of Schleswig-Holstein, Campus Kiel, Germany.

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.

Google Scholar

Google Scholar

Dimensions

Altmetric

PlumX Metrics

Downloads

Download data is not yet available.
Published
2011-05-06
Info
Issue
Section
Case Reports
Keywords:
temporobasal encephalomeningocele, neurosurgical removal, congenital defect, headache.
Statistics
  • Abstract views: 1302

  • PDF: 139
  • HTML: 218
How to Cite
Petridis, A. K., Doukas, A., & Mehdorn, H. M. (2011). A case of idiopathic encephalomeningocele. Clinics and Practice, 1(2), e29. https://doi.org/10.4081/cp.2011.e29