Department of Neurosurgery, University Hospital Basel, University of Basel, Basel, Switzerland.
Department of Neurosurgery, University Hospital Basel, University of Basel, Basel, Switzerland; Department of Oto-Rhino-Laryngology, Kantonsspital Graubünden, Chur, Switzerland.
World Neurosurg. 2024 Sep;189:456-464.e1. doi: 10.1016/j.wneu.2024.07.013. Epub 2024 Jul 8.
Recurrent cerebrospinal fluid (CSF) rhinorrhea caused by sequential, anatomically separated skull base defects is rarely reported in the literature. Neither management nor etiology has been sufficiently investigated. We present an illustrative case and a systematic review of the literature regarding etiology, diagnostics, and management of this rare phenomenon.
A systematic literature search looking for articles reporting sequential CSF leaks with multiple skull base defects was performed. Data from included articles were descriptively reported, and the quality of the included studies was assessed with Grading of Recommendations Assessment, Development and Evaluation.
A 71-year-old woman with posttraumatic CSF rhinorrhea and left-sided CSF otorrhea due to a left-sided horizontal fracture of the petrous bone presented at our institution. After initial surgical repair and a 10-week symptom-free interval, CSF rhinorrhea recurred. Imaging revealed a preexisting contralateral meningoencephalocele of the lateral sphenoid recess causing recurrent CSF rhinorrhea most likely after initial traumatic laceration. The defect was successfully treated. A literature search identified 366 reports, 6 of which were included in the systematic review with a total of 10 cases. Quality was deemed good in 8 of 10 cases. The most common location for primary and sequential CSF leaks was along the sphenoid bone (4/10 and 5/10 patients, respectively). All publications except one reported the presence of a meningo (encephalo)cele as cause of the sequential CSF leak.
Occurrence of recurrent CSF rhinorrhea due to an anatomically separated sequential skull base lesion remains a rare phenomenon. Reassessment of imaging studies and a structured diagnostic workup to detect sequential CSF leaks independent of the primary lesion should is recommended.
由相继发生的、解剖位置分离的颅底缺陷引起的复发性脑脊液(CSF)鼻漏在文献中很少报道。其管理和病因尚未得到充分研究。我们报告了一个说明性病例,并对文献进行了系统回顾,以了解这种罕见现象的病因、诊断和治疗。
我们进行了系统的文献检索,寻找报告多个颅底缺陷并发 CSF 漏的文章。对纳入文章的数据进行描述性报告,并使用推荐评估、制定与评估分级(Grading of Recommendations Assessment, Development and Evaluation)评估纳入研究的质量。
一名 71 岁女性,因左岩骨水平骨折导致创伤性 CSF 鼻漏和左侧 CSF 耳漏就诊于我院。初始手术修复后 10 周无症状期后,CSF 鼻漏再次发生。影像学显示存在先前存在的对侧蝶骨外侧隐窝脑膜脑膨出,最初创伤性撕裂后最有可能导致 CSF 鼻漏复发。该缺陷得到成功治疗。文献检索确定了 366 份报告,其中 6 份报告被纳入系统综述,共有 10 例。10 例中有 8 例质量被认为良好。原发性和继发性 CSF 漏的最常见位置是蝶骨(分别为 4/10 和 5/10 例患者)。除 1 篇文献外,所有文献均报告存在脑膜(脑)膨出是继发性 CSF 漏的原因。
由于解剖位置分离的相继颅底病变导致复发性 CSF 鼻漏仍然是一种罕见现象。建议重新评估影像学研究,并进行结构化的诊断检查,以独立于原发性病变检测继发性 CSF 漏。