Kennedy Richard J, Shelton Clough, Salzman Karen L, Davidson H Christian, Harnsberger H Ric
Department of Otolaryngology, University of Utah, Salt Lake City, Utah 84132, USA.
Otol Neurotol. 2004 Mar;25(2):160-7. doi: 10.1097/00129492-200403000-00014.
To outline the diagnosis and management of intralabyrinthine schwannomas and to propose a new classification system to further define them.
Retrospective case review.
Tertiary referral center at a university hospital.
Twenty-eight patients seen at the institution with intralabyrinthine schwannomas between 1996 and 2002 were included in the study.
Diagnosis was made with magnetic resonance imaging in all but one case. Our ability to detect these tumors has been greatly enhanced by the introduction of high-resolution T2-weighted magnetic resonance imaging. Treatment options were observation with serial magnetic resonance imaging versus complete surgical removal via a translabyrinthine or transotic approach. Surgery was indicated for dizziness caused by the tumor or extralabyrinthine growth.
Clinical features, audiology, radiology, and management outcomes were evaluated.
Eight patients have undergone successful surgery with removal of their tumors and resolution of symptoms. One patient chose to have stereotactic radiotherapy. Of the 20 patients who were managed with observation and serial magnetic resonance imaging, only 1 has shown significant growth requiring surgical removal.
Intralabyrinthine schwannomas are uncommon tumors that mimic the clinical features of many other neurotologic conditions. A high index of suspicion and precise imaging are often required to detect these tumors. Surgical treatment is indicated for specific indications and will be needed in the minority of patients with this disorder. The classification system that we propose is helpful in both the diagnosis and the management of these tumors.
概述迷路内神经鞘瘤的诊断与治疗,并提出一种新的分类系统以进一步明确此类肿瘤。
回顾性病例分析。
大学医院的三级转诊中心。
纳入1996年至2002年间在该机构就诊的28例迷路内神经鞘瘤患者。
除1例患者外,所有患者均通过磁共振成像进行诊断。高分辨率T2加权磁共振成像技术的引入极大地提高了我们检测这些肿瘤的能力。治疗方案包括通过系列磁共振成像观察与经迷路或经耳道入路完全手术切除。因肿瘤导致头晕或存在迷路外生长时则需进行手术。
评估临床特征、听力学、放射学及治疗效果。
8例患者成功接受手术切除肿瘤并症状缓解。1例患者选择立体定向放射治疗。在20例接受观察及系列磁共振成像检查的患者中,仅1例出现显著生长需要手术切除。
迷路内神经鞘瘤是罕见肿瘤,其临床特征与许多其他耳科疾病相似。检测这些肿瘤通常需要高度怀疑并进行精确成像。针对特定指征需进行手术治疗,且该疾病的少数患者需要手术。我们提出的分类系统有助于此类肿瘤的诊断与治疗。