Mulcahy M M, McMenomey S O, Talbot J M, Delashaw J B
Department of Otolaryngology-Head and Neck Surgery, Oregon Health Sciences University, Portland 97201, USA.
Laryngoscope. 1997 Jul;107(7):910-4. doi: 10.1097/00005537-199707000-00014.
Meningoencephaloceles of the temporal bone are rare. Although most often seen following otologic surgery or trauma, congenital meningoencephaloceles can exist. The clinical presentation, diagnostic evaluation, and surgical management of three patients with congenital meningoencephalocele are presented. Two of the three patients presented to our institution with recurrent episodes of meningitis; one presented with partial complex seizures. Diagnostic evaluation included temporal bone computed tomography with magnetic resonance imaging. In two patients, defects were imaged following high-pressure subarachnoid cisternography with computed tomography. All three patients were found to have congenital defects in the area of Meckel's cave. Early recognition of congenital meningoencephalocele is important to avoid delay of definitive surgical management and neurologic sequelae.
颞骨脑膜脑膨出较为罕见。虽然最常见于耳科手术后或外伤后,但先天性脑膜脑膨出也可能存在。本文介绍了3例先天性脑膜脑膨出患者的临床表现、诊断评估及手术治疗情况。3例患者中有2例因反复发生脑膜炎就诊于我院;1例表现为部分性复杂癫痫发作。诊断评估包括颞骨计算机断层扫描及磁共振成像。2例患者在高压蛛网膜下腔脑池造影后行计算机断层扫描时发现了缺损。所有3例患者均在梅克尔腔区域发现先天性缺损。早期识别先天性脑膜脑膨出对于避免确定性手术治疗的延迟及神经后遗症很重要。