Peris-Celda Maria, Graffeo Christopher S, Perry Avital, Carlstrom Lucas P, Link Michael J
Department of Neurologic Surgery, Mayo Clinic, Rochester, Minnesota, United States.
Department of Otolaryngology-Head and Neck Surgery, Mayo Clinic, Rochester, Minnesota, United States.
J Neurol Surg B Skull Base. 2018 Dec;79(Suppl 5):S389-S390. doi: 10.1055/s-0038-1669966. Epub 2018 Sep 25.
Large and even moderate sized, extra-axial cerebellopontine angle (CPA) tumors may fill this restricted space and distort the regional anatomy. It may be difficult to determine even with high resolution magnetic resonance imaging (MRI) if the tumor is dural-based, or what the nerve of origin is if a schwannoma. While clinical history and exam are helpful, they are not unequivocal, particularly since many patients present with a myriad of symptoms, or conversely an incidental finding. We present an atypical appearing, asymptomatic CPA tumor, ultimately identified at surgery to be a trigeminal schwannoma. A 40-year-old man presented with new-onset seizure. MRI identified an incidental heterogeneously contrast-enhancing CPA lesion ( Fig. 1A - D ). The tumor was centered on the internal auditory canal (IAC) with no tumor extension into Meckel's cave, IAC or jugular foramen. Audiometry demonstrated 10db of relative left-sided hearing loss with 100% word recognition. Physical examination was negative for focal neurologic deficits. A retrosigmoid craniotomy was performed and an extra-axial, yellow-hued mass was encountered and resected, which was ultimately confirmed to originate from the trigeminal nerve ( Video 1 ). Gross total resection was achieved, and the patient recovered from surgery with partial ipsilateral trigeminal sensory loss and no other new neurologic deficits. Pure CPA trigeminal schwannomas are rare, but should be considered in the differential for enhancing CPA lesions. Although, Meckel's cave involvement is frequently observed, it is not universal, and pure CPA schwannomas of all cranial nerves IV-XII have been reported in the literature. The link to the video can be found at: https://youtu.be/AlodYCu70F8 .
大型甚至中等大小的桥小脑角(CPA)区轴外肿瘤可能会占据这个有限的空间并使局部解剖结构变形。即使使用高分辨率磁共振成像(MRI),也可能难以确定肿瘤是否起源于硬脑膜,或者如果是神经鞘瘤,其起源神经是什么。虽然临床病史和检查有帮助,但并不明确,特别是因为许多患者表现出各种各样的症状,或者相反是偶然发现。我们报告一例外观不典型、无症状的CPA区肿瘤,最终在手术中确定为三叉神经鞘瘤。
一名40岁男性因新发癫痫就诊。MRI发现一个偶然的不均匀强化的CPA区病变(图1A - D)。肿瘤以内耳门(IAC)为中心,没有肿瘤延伸至 Meckel 腔、IAC 或颈静脉孔。听力测试显示左侧相对听力损失10dB,单词识别率为100%。体格检查未发现局灶性神经功能缺损。进行了乙状窦后开颅手术,遇到并切除了一个轴外的黄色肿块,最终证实其起源于三叉神经(视频1)。实现了肿瘤全切,患者术后恢复,出现同侧部分三叉神经感觉丧失,无其他新的神经功能缺损。
单纯的CPA区三叉神经鞘瘤很少见,但在鉴别强化的CPA区病变时应予以考虑。虽然,Meckel腔受累很常见,但并非普遍存在,文献中已报道了所有第IV - XII对脑神经单纯的CPA区神经鞘瘤。视频链接可在:https://youtu.be/AlodYCu70F8 找到。