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[涉及鼓室盖缺损的自发性耳漏]

[Spontaneous otorrhea involving defects of the tegmentum tympani].

作者信息

Page C, Peltier J, Strunski V, Legars D

机构信息

Laboratoire d'anatomie et d'organogenèse à la faculté de médecine et Service d'ORL et de chirurgie cervico-faciale, C.H.U., Hôpital Nord, Place Victor Pauchet, 80054 Amiens Cedex 1.

出版信息

Ann Otolaryngol Chir Cervicofac. 2004 Nov;121(5):298-302. doi: 10.1016/s0003-438x(04)95524-7.

Abstract

OBJECTIVE

We report two cases and a review of the literature concerning spontaneous otoliquorrhea involving congenital bone defects of the tegmen tympani.

CASE REPORTS

Both patients were managed by a cooperative otological and neurosurgical team. Otological symptoms predominated. The bilateral bone defects of the tegmen tympani were highlighted by high-resolution computed tomography. Surgery was undertaken via the middle fossa approach.

DISCUSSION

Spontaneous cerebrospinal fluid otorrhea related to tegmen tympani defects is rare. It occurs in adults with no previous otological history. The anomaly is congenital. Otological symptoms (differential diagnosis with serous media otitis) are usually predominant. Infectious meningitis may occur. The diagnosis is based on high resolution computed tomography and surgical treatment is required. Numerous technical approaches are possible (transmastoid and/or middle fossa approach) depending on the extent of the defect. Complete recovery is usual after adapted surgical treatment.

摘要

目的

我们报告两例病例,并对有关涉及鼓室盖先天性骨缺损的自发性耳漏的文献进行综述。

病例报告

两名患者均由耳科和神经外科合作团队进行治疗。耳科症状较为突出。高分辨率计算机断层扫描突出显示了双侧鼓室盖骨缺损。手术通过中颅窝入路进行。

讨论

与鼓室盖缺损相关的自发性脑脊液耳漏很少见。它发生在既往无耳科病史的成年人中。这种异常是先天性的。耳科症状(与浆液性中耳炎的鉴别诊断)通常较为突出。可能会发生感染性脑膜炎。诊断基于高分辨率计算机断层扫描,且需要进行手术治疗。根据缺损的范围,有多种技术方法可行(经乳突和/或中颅窝入路)。经过适当的手术治疗后通常可完全康复。

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