Hervey-Jumper Shawn L, Ghori Ahmer K, Quint Douglas J, Marentette Lawrence J, Maher Cormac O
Department of Neurosurgery, University of Michigan, Ann Arbor, Michigan 48109-5338, USA.
J Neurosurg Pediatr. 2010 Mar;5(3):302-5. doi: 10.3171/2009.10.PEDS09336.
The authors report an unusual case of bilateral large petrous apex cephaloceles in a 14-year-old boy with a history of recurrent meningitis. Although these lesions are rare and usually asymptomatic, surgical correction is recommended if they are associated with a persistent CSF leak. In this patient, the extensive bilateral cranial defects were not adequately treated by an intracranial approach alone. Repair of a defect in the posterior pharyngeal wall, the site of a prior tonsillectomy, ultimately resulted in repair of the CSF fistula.
作者报告了一例不同寻常的病例,一名14岁有复发性脑膜炎病史的男孩患有双侧巨大岩尖脑膨出。尽管这些病变罕见且通常无症状,但如果与持续性脑脊液漏相关,则建议进行手术矫正。在该患者中,单纯采用颅内入路并不能充分治疗广泛的双侧颅骨缺损。修复咽后壁(先前扁桃体切除术部位)的缺损最终成功修复了脑脊液瘘。