Englhard Anna S, Volgger Veronika, Leunig Andreas, Meßmer Catalina S, Ledderose Georg J
Department of Otorhinolaryngology-Head and Neck Surgery, Klinikum der Universität München, Marchioninistr. 15, 81377, Munich, Germany.
Rhinology Center, ENT-Clinic Bogenhausen, Dr. Gaertner GmbH, Munich, Germany.
Eur Arch Otorhinolaryngol. 2018 Oct;275(10):2487-2494. doi: 10.1007/s00405-018-5089-y. Epub 2018 Aug 14.
Most cases of non-traumatic nasal cerebrospinal fluid (CSF) leaks occur spontaneously without any obvious reason. Severe and life-threatening complications are possible consequences. Endoscopic repair is considered the gold standard; however, diagnosis and therapy of these CSF leaks stay challenging.
In this retrospective analysis, patients who presented with spontaneous nasal CSF leaks from 2006 to 2017 were included. Symptoms, diagnostics, localization of the skull base defect, surgical method, outcome, and postoperative treatment were recorded.
Twenty four patients were included. 8 patients presented with symptoms of meningitis. The skull base defects were most commonly located in the anterior ethmoid roof-especially in the cribriform plate-and in the lateral part of the sphenoid sinus. 21 patients had a BMI above 25. In only 13 cases the defect could be detected preoperatively via computed tomography or additional magnetic resonance imaging. In all patients intraoperative visualization of the CSF leak was possible using intrathecal application of sodium-fluorescein. Endoscopic repair was the initial surgical method for all patients and proved to be successful in 80% of the cases. In most cases surgical revision was performed endoscopically; however, in two patients an open transpterygoidal approach was necessary.
Spontaneous nasal CSF leaks often initially present with symptomatic meningitis. Imaging does not always clearly identify the skull base defect. Common localizations are the anterior ethmoid roof and the lateral sphenoid sinus. Obesity seems to be a predisposing factor. In most cases, endoscopic repair with low morbidity is possible; however, an individualized approach is necessary.
大多数非创伤性鼻脑脊液漏病例无明显原因自发发生。严重且危及生命的并发症可能随之而来。内镜修复被认为是金标准;然而,这些脑脊液漏的诊断和治疗仍然具有挑战性。
在这项回顾性分析中,纳入了2006年至2017年出现自发性鼻脑脊液漏的患者。记录症状、诊断、颅底缺损的定位、手术方法、结果和术后治疗情况。
纳入24例患者。8例患者出现脑膜炎症状。颅底缺损最常见于筛窦前壁顶部,尤其是筛板,以及蝶窦外侧部分。21例患者体重指数高于25。仅13例患者术前通过计算机断层扫描或额外的磁共振成像检测到缺损。所有患者术中通过鞘内注射荧光素钠均可观察到脑脊液漏。内镜修复是所有患者的初始手术方法,80%的病例证明成功。大多数病例通过内镜进行手术翻修;然而,有2例患者需要采用经翼点开放入路。
自发性鼻脑脊液漏通常最初表现为有症状的脑膜炎。影像学检查并不总是能清晰识别颅底缺损。常见的定位是筛窦前壁顶部和蝶窦外侧。肥胖似乎是一个诱发因素。在大多数情况下,内镜修复发病率低是可行的;然而,需要个体化治疗方法。