Wind Joshua J, Caputy Anthony J, Roberti Fabio
Department of Neurological Surgery, George Washington University, Washington, DC, USA.
Neurosurg Focus. 2008;25(6):E11. doi: 10.3171/FOC.2008.25.12.E11.
Encephaloceles are pathological herniations of brain parenchyma through congenital or acquired osseus-dural defects of the skull base or cranial vault. Although encephaloceles are known as rare conditions, several surgical reports and clinical series focusing on spontaneous encephaloceles of the temporal lobe may be found in the otological, maxillofacial, radiological, and neurosurgical literature. A variety of symptoms such as occult or symptomatic CSF fistulas, recurrent meningitis, middle ear effusions or infections, conductive hearing loss, and medically intractable epilepsy have been described in patients harboring spontaneous encephaloceles of middle cranial fossa origin. Both open procedures and endoscopic techniques have been advocated for the treatment of such conditions. The authors discuss the pathogenesis, diagnostic assessment, and therapeutic management of spontaneous temporal lobe encephaloceles. Although diagnosis and treatment may differ on a case-by-case basis, review of the available literature suggests that spontaneous encephaloceles of middle cranial fossa origin are a more common pathology than previously believed. In particular, spontaneous cases of posteroinferior encephaloceles involving the tegmen tympani and the middle ear have been very well described in the medical literature.
脑膨出是脑实质通过颅底或颅顶先天性或后天性骨质 - 硬膜缺损的病理性疝出。尽管脑膨出被认为是罕见病症,但在耳科学、颌面外科学、放射学和神经外科学文献中可以找到一些专注于颞叶自发性脑膨出的手术报告和临床系列。患有中颅窝起源的自发性脑膨出的患者出现了多种症状,如隐匿性或有症状的脑脊液漏、复发性脑膜炎、中耳积液或感染、传导性听力损失以及药物难治性癫痫。开放手术和内镜技术都被推荐用于治疗此类病症。作者讨论了自发性颞叶脑膨出的发病机制、诊断评估和治疗管理。虽然诊断和治疗可能因具体病例而异,但对现有文献的回顾表明,中颅窝起源的自发性脑膨出是一种比以前认为的更常见的病理情况。特别是,涉及鼓室盖和中耳的后下脑膨出自发性病例在医学文献中已有非常详细的描述。