Rose Oliver, Neeff Michel, Low Christopher
Auckland City Hospital, Auckland 1042, New Zealand.
Case Rep Otolaryngol. 2013;2013:969762. doi: 10.1155/2013/969762. Epub 2013 Oct 29.
Spontaneous tegmen tympani defects are rare with even rarer bilateral cases. The symptoms are nonspecific; hence, a high index of suspicion is required to prevent serious intracranial complications. We present a case of spontaneous bilateral tegmen tympani defects with associated meningoencephalocoeles in a 54-year-old male who presented with the signs and symptoms of severe meningitis. After careful workup which included a lumbar puncture, CT and MRI scans, both defects were repaired using a middle fossa approach. The patient made an uneventful recovery with complete cessation of otorrhoea and improvement in his hearing.
自发性鼓室盖缺损罕见,双侧病例更为罕见。症状不具特异性;因此,需要高度怀疑以预防严重的颅内并发症。我们报告一例54岁男性自发性双侧鼓室盖缺损伴脑膜脑膨出的病例,该患者表现出严重脑膜炎的体征和症状。经过包括腰椎穿刺、CT和MRI扫描在内的仔细检查后,采用中颅窝入路修复了两个缺损。患者恢复顺利,耳漏完全停止,听力有所改善。