Petridis Athanasios K, Doukas Alexandros, Mehdorn Hubertus M
Department of Neurosurgery, University Hospital of Schleswig-Holstein, Campus Kiel, Germany.
Clin Pract. 2011 May 6;1(2):e29. doi: 10.4081/cp.2011.e29. eCollection 2011 May 16.
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.
在本病例中,我们报告了一名成年女性的脑膨出合并脑膜膨出。由于这种医学病症的病因是颅底神经管的先天性融合缺陷,大多数脑膨出发生在儿童身上,导致面部畸形。在成人中描述的罕见病例中,通常会出现鼻漏。在此,我们呈现一例72岁女性患者的颞底部脑膨出合并脑膜膨出,该患者在过去4至5年中一直遭受头痛困扰。未发现鼻漏或其他明显的神经系统症状。未发现明显的先天性病因。经过包括脑磁共振成像(MRI)、头颅计算机断层扫描(CT)和磁共振脑池造影在内的诊断步骤后,确诊为脑膨出合并脑膜膨出。通过翼点入路将其完全切除。患者术后唯一抱怨的症状,即头痛,得以消除。