Division of Head and Neck Surgery, Department of Surgery, Queen Mary Hospital, University of Hong Kong Medical Centre, Pokfulam, Hong Kong, SAR, China.
Eur Arch Otorhinolaryngol. 2011 Sep;268(9):1343-7. doi: 10.1007/s00405-011-1491-4. Epub 2011 Jan 19.
Schwannoma is a type of benign nerve sheath tumour arising from the Schwann cell. Because of the close relationship between the tumour and the nerve of origin (NOO), the operation of extracranial head and neck schwannoma may lead to palsy of major nerve. For this reason, an accurate diagnosis of schwannoma with the identification of the NOO is crucial to the management. The aim of this review was to find out the distribution of the NOO and the usefulness of the investigations in the diagnosis of schwannoma. Medical records of the patients who underwent operation of the extracranial head and neck schwannoma in our division were reviewed. Between January 2000 and December 2009, 30 cases of extracranial head and neck schwannoma were operated. Sympathetic trunk (10, 33%) and vagus nerve (6, 20%) were the two most common NOOs. In five (17%) cases, the NOO was not found to be arising from any major nerve. For these 30 patients, 20 received fine needle aspiration cytology (FNAC) and 26 underwent imaging studies (computed tomography or magnetic resonance imaging) before operation. The specificity of FNAC and imaging studies in making the diagnosis of schwannoma was 20 and 38%, respectively. For the patients who had nerve palsies on presentation, their deficits remained after operation. The rate of nerve palsy after tumour excision with division of NOO and intracapsular enucleation was 100 and 67%, respectively. The diagnosis of schwannoma is suggested by clinical features and supported by investigations. Most of the time, the diagnosis can only be confirmed on the histological study of the surgical specimen. Sympathetic trunk and vagus nerve are the two common NOOs. MRI is the investigation of choice in the diagnosis of schwannoma and the identification of NOO.
神经鞘瘤是一种起源于施万细胞的良性神经鞘肿瘤。由于肿瘤与起源神经(NOO)密切相关,颅外头颈部神经鞘瘤的手术可能导致主要神经麻痹。因此,准确诊断神经鞘瘤并识别 NOO 对治疗至关重要。本综述旨在探讨 NOO 的分布及各种检查在神经鞘瘤诊断中的作用。回顾性分析 2000 年 1 月至 2009 年 12 月在我科行颅外头颈部神经鞘瘤手术的患者病历。共手术治疗 30 例颅外头颈部神经鞘瘤,其中交感神经干(10 例,33%)和迷走神经(6 例,20%)是最常见的 NOO。5 例(17%)NOO 未发现来自任何主要神经。这 30 例患者中,20 例行细针抽吸细胞学检查(FNAC),26 例行影像学检查(计算机断层扫描或磁共振成像)。FNAC 和影像学检查诊断神经鞘瘤的特异性分别为 20%和 38%。对于有神经麻痹的患者,手术后神经缺损仍然存在。切除肿瘤时分离 NOO 和囊内剜除的神经麻痹发生率分别为 100%和 67%。神经鞘瘤的诊断依据临床特征,并辅以检查。大多数情况下,只有通过手术标本的组织学研究才能确诊。交感神经干和迷走神经是两种常见的 NOO。MRI 是诊断神经鞘瘤和识别 NOO 的首选检查方法。