Zhang Shaoxing, Ma Furong, Li Zhesheng, Wu Haibo
Department of Otorhinolaryngology-Head and Neck Surgery, Peking University Third Hospital, Beijing, 100191, China.
Department of Medical Imageology and Nuclear Medicine, Peking University Third Hospital.
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2013 Oct;27(19):1058-62, 1067.
To explore the clinical characteristics, diagnosis and surgical management of petrous bone cholesteatoma.
The data of 12 patients who underwent surgery for petrous bone cholesteatoma(PBC) were retrospectively analyzed with respects to the clinical characteristics, diagnosis and management.
Seven cases were characterized by a long otitis media history, severe hearing loss, and facial paralysis. In contrast, 5 cases were characterized with the symptoms of facial paralysis, hearing loss and vertigo attack and the absence of early otorrhea history. Trans labyrinth approach was chosen for 2 cases,while trans labyrinth-cochlear approach for 10. Cochlea was involved in 10 cases, while internal auditory canal in 9 and semicircular canal in 11. Otoscope was used in 1 case. Four patients were treated by partial resection of petrous apex and ear canal closure with good results. After years of follow-up, three recurrence cases were operated for a second time. Simultaneous facial nerve anastomosis or decompression was performed. The function of facial nerve recovered from V-VI to Ill-IV (House and Brackmann grading) in 6 anastomosis cases and from IV-V to II- IlI in 3 cases of decompression.
Petrous bone cholesteatoma was characterized by severe hearing loss, and facial paralysis. Surgical approaches are decided according to the extent of lesion and hearing status. Our study indicated that otoscope would help to ensure a radical removal of the pathology in cases with deep involvement and restricted vision. Partial resection of petrous bone and ear canal closure could be effective solution for challenging cerebrospinal fluid otorrhea with large dural defects and protecting vital neurovascular structures.
探讨岩骨胆脂瘤的临床特征、诊断及手术治疗方法。
回顾性分析12例接受岩骨胆脂瘤(PBC)手术患者的临床特征、诊断及治疗资料。
7例患者有长期中耳炎病史、重度听力损失及面瘫。相比之下,5例患者表现为面瘫、听力损失及眩晕发作,且无早期耳漏病史。2例患者采用经迷路入路,10例采用经迷路-耳蜗入路。10例患者耳蜗受累,9例患者内耳道受累,11例患者半规管受累。1例患者使用了耳镜。4例患者行岩尖部分切除术并外耳道封闭,效果良好。经过多年随访,3例复发患者再次接受手术。同时进行了面神经吻合或减压。6例吻合患者面神经功能从Ⅴ级恢复至Ⅲ-Ⅳ级(House和Brackmann分级),3例减压患者面神经功能从Ⅳ-Ⅴ级恢复至Ⅱ-Ⅲ级。
岩骨胆脂瘤以重度听力损失及面瘫为特征。手术入路根据病变范围及听力状况决定。我们的研究表明,在病变累及较深且视野受限的情况下,耳镜有助于确保彻底切除病变。岩骨部分切除术及外耳道封闭对于伴有大的硬脑膜缺损的挑战性脑脊液耳漏及保护重要神经血管结构可能是有效的解决方法。