斜坡缺损致自发性脑脊液鼻漏1例报告及文献复习。

IF 0.4 Q4 OTORHINOLARYNGOLOGY
Maryam Aljawi, Mahdi Shkoukani
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引用次数: 0

摘要

自发性脑脊液(CSF)鼻漏发生在没有任何外伤史的患者。多种因素在理论上一直存在争议。此外,定位缺陷可能会给鼻医生带来挑战。常见的位置是筛状板和蝶骨外侧隐窝。Clival CSF鼻漏是一种罕见的疾病,目前仅有少数病例报道。52岁女性,就诊于耳鼻喉科门诊,左侧透明液体性鼻漏7年,呈滴状,感染COVID-19继发严重咳嗽肺炎后进展为流涕。脑脊液经-2-转铁蛋白试验证实。围手术期评估中,患者出现脑膜炎,经静脉注射头孢曲松和万古霉素抗生素治疗。磁共振成像(MRI)和计算机断层扫描(CT)显示斜坡缺损伴假性脑膜膨出,最初在CT上不易发现。病人接受内窥镜入路到颅底用带蒂鼻中隔皮瓣修复缺损。同时,采用鞘内荧光素给药腰椎引流。术后过程顺利,无任何并发症。术后9个月随访无复发迹象。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Clival Defect Resulting in Spontaneous Cerebrospinal Fluid Rhinorrhea: Case Report and Review of Literature.

Clival Defect Resulting in Spontaneous Cerebrospinal Fluid Rhinorrhea: Case Report and Review of Literature.

Clival Defect Resulting in Spontaneous Cerebrospinal Fluid Rhinorrhea: Case Report and Review of Literature.

Clival Defect Resulting in Spontaneous Cerebrospinal Fluid Rhinorrhea: Case Report and Review of Literature.

Spontaneous cerebrospinal fluid (CSF) rhinorrhea develops in patients without any history of trauma. Multiple factors have been theoretically debated. Also, localizing the defect may result in a challenge for the rhinologist. The common locations are the cribriform plate and the lateral recess of the sphenoid. Clival CSF rhinorrhea is rare, and only few cases have been reported so far. A 52-year-old female presented to the otolaryngology clinic with 7 years of history of left-side clear fluid rhinorrhea as a drop, which progressed to be runnier after she had pneumonia with severe cough secondary to COVID-19 infection. CSF was confirmed by a beta-2-transferrin test. During the perioperative evaluation, she developed meningitis which was treated with IV ceftriaxone and IV vancomycin antibiotics. The magnetic resonance imaging (MRI) and computerized tomography (CT) scan showed clival defect with pseudomeningocele which was initially not easy to see on CT. The patient underwent an endoscopic approach to the skull base to repair the defect with a pedicled septal flap. Also, a lumbar drain with intrathecal fluorescein administration was utilized. The postoperative course was uneventful without any complications. There was no evidence of recurrence with a 9-month follow-up postoperatively.

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来源期刊
Case Reports in Otolaryngology
Case Reports in Otolaryngology OTORHINOLARYNGOLOGY-
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审稿时长
13 weeks
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