Moe K S, Li D, Linder T E, Schmid S, Fisch U
Skull Base Surg. 1999;9(3):185-94. doi: 10.1055/s-2008-1058145.
In 1982, Fisch described his results for the surgical treatment of 74 paragangliomas of the temporal bone, 5 years after his description of the infratemporal fossa approaches (types A and B). This study reviews the subsequent experience of the Department of Otolaryngology-Head and Neck Surgery of the University of Zürich with more than 136 surgically treated cases of paraganglioma of the temporal bone and discusses our current therapy 20 years after the initial description. One hundred nineteen (90%) of the patients had advanced tumors (Fisch class C or C+D), and 81 (68%) had intracranial extension. Total tumor excision was possible in 109 (82%) patients. Subtotal excision was performed in 22 (17%) patients, 21 of whom had intradural tumor invasion. In these cases, the resection was limited not by actual tumor size but by the degree of intracranial intradural tumor extension. Partial tumor excision was undertaken in only 1 patient with a C4De2Di2 tumor. The success rate in preservation of function of the lower cranial nerves was encouraging. Of the 69 patients whose facial nerve status was followed post-operatively, 81% maintained Fisch grade 76 to 100% (House-Brackman grades I and II). Analysis of follow-up data ranging from 2 to 11 years demonstrated 98% disease-free survival when total tumor extirpation was possible. In the patients who underwent subtotal or partial surgical resection there has been no subsequent tumor growth detected by either clinical or neuroradiological evaluation. We have confirmed after more than 20 years of experience that the infratemporal fossa approaches are a safe, highly effective means of surgical management of paragangliomas of the temporal bone, allowing eradication or arrest of disease with minimal morbidity. Limited intradural surgical resection in cases of very extensive tumors can greatly benefit patients for whom complete excision is not an option.
1982年,菲施在描述了颞下窝入路(A类和B类)5年后,报告了他对74例颞骨副神经节瘤的手术治疗结果。本研究回顾了苏黎世大学耳鼻咽喉头颈外科对136例以上经手术治疗的颞骨副神经节瘤的后续经验,并讨论了自最初描述20年后我们目前的治疗方法。119例(90%)患者患有晚期肿瘤(菲施C级或C+D级),81例(68%)有颅内扩展。109例(82%)患者实现了肿瘤全切。22例(17%)患者进行了次全切除,其中21例有硬膜内肿瘤侵犯。在这些病例中,切除受限并非实际肿瘤大小,而是颅内硬膜内肿瘤扩展程度。仅1例C4De2Di2肿瘤患者进行了部分肿瘤切除。低位颅神经功能保留成功率令人鼓舞。69例术后随访面神经状态的患者中,81%维持菲施76%至100%的分级(House-Brackman I级和II级)。对2至11年随访数据的分析表明,肿瘤全切时无病生存率为98%。在接受次全或部分手术切除的患者中,临床或神经放射学评估均未发现后续肿瘤生长。经过20多年的经验,我们证实颞下窝入路是手术治疗颞骨副神经节瘤的一种安全、高效的方法,能以最小的发病率根除或控制疾病。对于无法全切的广泛肿瘤病例,有限的硬膜内手术切除可使患者受益匪浅。