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来自颅中窝和后颅窝缺损的自发性脑脊液耳漏。

Spontaneous CSF otorrhea from tegmen and posterior fossa defects.

作者信息

Ferguson B J, Wilkins R H, Hudson W, Farmer J

出版信息

Laryngoscope. 1986 Jun;96(6):635-44. doi: 10.1288/00005537-198606000-00009.

Abstract

Spontaneous cerebrospinal otorrhea (SCSFO) from tegmen or posterior fossa defects is uncommon. Twenty-nine cases have been detailed in the literature to date. We report an additional four cases from three patients. This group of 33 cases of SCSFO from tegmen or posterior fossa defects is characterized by certain clinical features. These patients are usually older adults (mean age 48 years, range 8 months to 80 years). Aural fullness with a serous appearing middle ear effusion, or clear otorrhea, often subsequent to tube myringotomy, are the usual initial symptoms. Meningitis was the initial manifestation in eight patients (24%), and ultimately occurred in an additional four patients (12%). The pathophysiologic basis for SCSFO from tegmen defects is discussed. Methods for diagnosing and treating CSF otorrhea from tegmen defects are reviewed.

摘要

来自颅中窝或后颅窝缺损的自发性脑脊液耳漏(SCSFO)并不常见。迄今为止,文献中已详细报道了29例。我们报告了另外3例患者的4个病例。这组33例来自颅中窝或后颅窝缺损的SCSFO具有某些临床特征。这些患者通常为老年人(平均年龄48岁,范围8个月至80岁)。通常最初的症状是鼓膜切开置管术后出现耳闷伴浆液性中耳积液或清亮耳漏。脑膜炎是8例患者(24%)的初始表现,最终又有4例患者(12%)发生脑膜炎。讨论了颅中窝缺损导致SCSFO的病理生理基础。回顾了诊断和治疗颅中窝缺损导致脑脊液耳漏的方法。

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