Braca John A, Marzo Sam, Prabhu Vikram C
Department of Neurological Surgery, Loyola University Medical Center, Maywood, Illinois, United States.
Department of Otolaryngology, Head and Neck Surgery, Loyola University Medical Center, Maywood, Illinois, United States.
J Neurol Surg B Skull Base. 2013 Apr;74(2):103-7. doi: 10.1055/s-0033-1333616. Epub 2013 Jan 22.
Spontaneous cerebrospinal fluid (CSF) otorrhea due to tegmen tympani defects can result in hearing impairment and predispose to meningitis. Seizures or neurological deficits are additional risks, particularly when associated with an encephalocele. Surgical repair of the dural defect through a middle cranial fossa (MCF) approach is a treatment option under these circumstances. This series describes eight individuals who presented with CSF otorrhea and MCF encephaloceles associated with conductive hearing loss. Defects in the tegmen tympani were noted in all patients on preoperative cranial imaging, and six of the eight patients had an associated encephalocele. The average age was 57 years (range 26 to 67) with a male:female ratio of 7:1. Most defects occurred on the left side (6 left/2 right). A standard MCF approach and repair of the dural defect with an autologous dural graft (Durepair or DuraGen, Medtronic, Minneapolis, Minnesota, USA) and a synthetic polymer glue (DuraSeal, Covidien, Mansfield, Massachusetts) was performed in each case with universal success. Resolution of the CSF otorrhea was noted in all cases. All cases but one exhibited an improvement in hearing. One patient developed a delayed methicillin-resistant Staphylococcus aureus meningitis 3 months after surgery that resolved with surgical re-exploration and antibiotic therapy. Facial nerve monitoring was standard. All patients exhibited normal facial function postoperatively. Prophylactic lumbar drain placement was only utilized in the first three patients. The MCF approach is an excellent route to effectively repair CSF leaks and encephaloceles due to tegmen tympani and dural defects.
由于鼓室盖缺损导致的自发性脑脊液耳漏可导致听力损害,并易引发脑膜炎。癫痫发作或神经功能缺损是额外的风险,尤其是与脑膨出相关时。在这种情况下,通过中颅窝(MCF)入路对硬脑膜缺损进行手术修复是一种治疗选择。本系列描述了8例出现脑脊液耳漏和与传导性听力损失相关的MCF脑膨出的患者。术前头颅影像学检查发现所有患者均存在鼓室盖缺损,8例患者中有6例伴有脑膨出。平均年龄为57岁(范围26至67岁),男女比例为7:1。大多数缺损发生在左侧(6例左侧/2例右侧)。每例均采用标准的MCF入路,并用自体硬脑膜移植物(Durepair或DuraGen,美敦力公司,明尼阿波利斯,明尼苏达州,美国)和合成聚合物胶水(DuraSeal,科维迪恩公司,曼斯菲尔德,马萨诸塞州)修复硬脑膜缺损,均取得成功。所有病例的脑脊液耳漏均得到解决。除1例患者外,所有病例的听力均有改善。1例患者术后3个月发生耐甲氧西林金黄色葡萄球菌脑膜炎,经手术再次探查和抗生素治疗后痊愈。面神经监测为常规操作。所有患者术后面部功能均正常。仅前3例患者放置了预防性腰大池引流管。MCF入路是有效修复因鼓室盖和硬脑膜缺损导致的脑脊液漏和脑膨出的极佳途径。