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小儿脑膜脑膨出与鼻阻塞:内镜修复病例

Pediatric meningoencephaloceles and nasal obstruction: a case for endoscopic repair.

作者信息

Kanowitz Seth J, Bernstein Joseph M

机构信息

Head & Neck Institute, Section of Nasal & Sinus Disorders, Cleveland Clinic, Cleveland, OH, United States.

出版信息

Int J Pediatr Otorhinolaryngol. 2006 Dec;70(12):2087-92. doi: 10.1016/j.ijporl.2006.08.007. Epub 2006 Oct 27.

Abstract

OBJECTIVES

Congenital anterior skull base defects with meningoencephaloceles causing nasal obstruction are rare clinical entities. Nasal obstruction in children may also be a symptom of multiple benign nasal and allergic disorders, making the initial diagnosis of meningoencephalocele difficult. Traditionally, skull base defects have been repaired via a bifrontal craniotomy approach. With the advent of pediatric endoscopic instrumentation, more of these lesions are accessible via an intranasal endoscopic approach, even in the infant population. However, owing to the rarity of these lesions, there is a paucity of data demonstrating successful adaptation of endoscopic skull base techniques to the pediatric population.

METHODS

Retrospective review of two cases of endoscopic repair of anterior skull base defects with meningoencephaloceles at a tertiary care medical center.

RESULTS

Two children, ages 15 months and 6 years, underwent successful endoscopic closure of their anterior skull base defects and resection of their intranasal meningoencephalocele with resolution of their nasal obstruction and cerebrospinal fluid rhinorrhea.

CONCLUSIONS

Pediatric nasal meningoencephaloceles with anterior skull base defects can be successfully repaired via a transnasal endoscopic technique, thus minimizing the complications associated with craniotomy and frontal lobe retraction. Triplanar computed tomographic and magnetic resonance imaging is paramount to evaluate the caliber of the skull base defect, consistency of the herniated intracranial contents, as well as the presence of cerebral vasculature.

摘要

目的

先天性前颅底缺损合并脑膜脑膨出导致鼻阻塞是一种罕见的临床病症。儿童鼻阻塞也可能是多种良性鼻部和过敏性疾病的症状,这使得脑膜脑膨出的初步诊断变得困难。传统上,颅底缺损通过双额开颅手术进行修复。随着小儿内镜器械的出现,即使在婴儿群体中,更多此类病变也可通过鼻内镜入路进行处理。然而,由于这些病变罕见,缺乏数据表明内镜颅底技术在儿科人群中的成功应用。

方法

对一家三级医疗中心两例前颅底缺损合并脑膜脑膨出的内镜修复病例进行回顾性分析。

结果

两名儿童,年龄分别为15个月和6岁,成功接受了内镜下前颅底缺损闭合术及鼻内脑膜脑膨出切除术,鼻阻塞和脑脊液鼻漏症状得以缓解。

结论

伴有前颅底缺损的小儿鼻脑膜脑膨出可通过经鼻内镜技术成功修复,从而将与开颅手术和额叶牵拉相关的并发症降至最低。三维计算机断层扫描和磁共振成像对于评估颅底缺损的大小、疝出颅内内容物的情况以及脑血管的存在至关重要。

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