Gerhardt H J, Mühler G, Szdzuy D, Biedermann F
Zentralbl Neurochir. 1979;40(1):85-94.
After a brief survey of the forms of cranial meningoencephaloceles, the current opinions on their development, symptoms and surgical therapy, a report is given on the case of a five-year-old boy suffering from a sphenoethmoidal meningocele of the size 3 x 3 x 4 cm. There was at the same time a wide median palate cleft, obviously a consequence of the meningoencephalocele. A further finding presented by the boy was a neuroradiologically diagnosed agenesis of the Corpus callosum and a median cheiloschisis. This suggests a central development disturbance as a primary cause. The attempt to perform an intracranial occlusion of the defect of the base, which was repeated twice, was not successful. It was only by a transpalatinal-transnasal extradural intervention (reposition of the meningocele after removing the epipharyngeal mucosa, blocking of the bony defect with a perforated tantalum plate) that the removal of the meningocele was successful. The closure of the palate cleft was then made by the oral surgeon. This surgical intervention may also be considered for the treatment of the transsphenoidal meningoencephalocele, which also presents many problems.
在简要概述颅脑膜脑膨出的形式、目前对其发育、症状及手术治疗的观点之后,报告了一例5岁男孩患有大小为3×3×4厘米的蝶筛脑膜膨出的病例。同时存在较宽的正中腭裂,显然是脑膜脑膨出的结果。该男孩的另一项检查结果是经神经放射学诊断为胼胝体发育不全及正中唇裂。这提示中枢发育障碍是主要病因。尝试对颅底缺损进行两次颅内封堵均未成功。仅通过经腭 - 经鼻硬膜外干预(切除咽上黏膜后将脑膜膨出复位,用带孔钽板封闭骨缺损)才成功切除脑膜膨出。然后由口腔外科医生闭合腭裂。这种手术干预也可考虑用于治疗经蝶窦脑膜脑膨出,经蝶窦脑膜脑膨出也存在许多问题。