Chung Jong Woo, Ahn Joong Ho, Kim Jae Ho, Nam Soon Yuhl, Kim Chang-Jin, Lee Kwang-Sun
Department of Otolaryngology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, South Korea.
Surg Neurol. 2004 Sep;62(3):245-52; discussion 452. doi: 10.1016/j.surneu.2003.09.034.
The purpose of this study was to provide data on the different clinical presentations of facial nerve schwannoma, the appropriate planning for the management of schwannoma of various origins, and the predictive outcomes of surgical management.
A retrospective study was conducted in a tertiary referral hospital. We reviewed 8 consecutive cases of facial nerve schwannoma diagnosed and managed between 1993 and 2001.
Facial nerve schwannomas originated in the internal auditory canal (IAC) (2 cases), parotid gland (2 cases), intratemporal portion (3 cases), and stylomastoid foramen (1 case). Tumor of the stylomastoid foramen presented as an intra- and extratemporal mass. The initial presenting symptom of the 8 patients was facial nerve paralysis in 4 patients, hearing loss in 2, facial numbness in 1, and an infra-auricular mass in 1. Facial palsy occurred in 7 patients during the course of the disease. One patient with a mass in the parotid gland did not show facial palsy up to 1 year after presentation of the initial symptom (facial numbness). Facial nerve paralysis was most severe in intratemporal tumors and less severe in parotid tumors. The patients with IAC suffered from hearing loss and intermittent vertigo and showed decreased vestibular function. The patients with intratemporal tumors also complained of hearing loss. The tumors were completely removed by superficial parotidectomy for parotid tumors; the translabyrinthine approach for 1 IAC tumor and 1 intratemporal tumor; the middle fossa approach for the other IAC tumor; the transmastoid approach for mastoid tumors; and the infratemporal fossa approach for intratemporal and extratemporal tumors. End-to-end cable grafts for the facial nerve were performed in 5 out of 8 cases. In 2 cases, the facial nerve was preserved after the resection of the mass. One case showed complete loss of the peripheral branch of the facial nerve.
Facial nerve schwannoma can present in various ways. By examining the site of origin and the presenting symptoms and signs, we were able to diagnose facial nerve schwannoma preoperatively. According to the operative management of the facial nerve, the postoperative outcome of facial function could be estimated. Our finding could be pivotal in the management of the facial nerve schwannoma.
本研究旨在提供有关面神经鞘瘤不同临床表现的数据,为各种起源的鞘瘤管理制定合适的方案,并预测手术治疗的结果。
在一家三级转诊医院进行了一项回顾性研究。我们回顾了1993年至2001年间连续诊断和治疗的8例面神经鞘瘤病例。
面神经鞘瘤起源于内耳道(IAC)(2例)、腮腺(2例)、颞内部分(3例)和茎乳孔(1例)。茎乳孔肿瘤表现为颞内和颞外肿块。8例患者的初始症状为4例面神经麻痹、2例听力丧失、1例面部麻木和1例耳下肿块。7例患者在病程中出现面神经麻痹。1例腮腺肿块患者在出现初始症状(面部麻木)后长达1年未出现面神经麻痹。面神经麻痹在颞内肿瘤中最为严重,在腮腺肿瘤中较轻。IAC患者出现听力丧失和间歇性眩晕,前庭功能下降。颞内肿瘤患者也主诉听力丧失。腮腺肿瘤通过浅叶腮腺切除术完全切除;1例IAC肿瘤和1例颞内肿瘤采用经迷路入路;另1例IAC肿瘤采用中颅窝入路;乳突肿瘤采用经乳突入路;颞内和颞外肿瘤采用颞下窝入路。8例中有5例进行了面神经端端电缆移植。2例在肿块切除后保留了面神经。1例显示面神经外周分支完全丧失。
面神经鞘瘤可表现为多种形式。通过检查起源部位以及出现的症状和体征,我们能够在术前诊断面神经鞘瘤。根据面神经的手术处理,可对面部功能的术后结果进行评估。我们的发现可能对面神经鞘瘤的管理至关重要。