Figueiredo Eberval Gadelha, Soga Yougi, Amorim Robson Luis Oliveira, Oliveira Arthur Maynart Pereira, Teixeira Manoel Jacobsen
Skull Base. 2011 Jan;21(1):31-6. doi: 10.1055/s-0030-1262945.
We systematically reviewed the literature concerning the anterior cranial fossa schwannomas to understand their pathogenesis, determine their origin, and standardize the terminology. We performed a MEDLINE, EMBASE, and Science Citation Index Expanded search of the literature; age, gender, clinical presentation, presence or absence of hyposmia, radiological features, and apparent origin were analyzed and tabulated. Cases in a context of neurofibromatosis and nasal schwannomas with intracranial extension were not included. Age varied between 14 and 63 years (mean = 30.9). There were 22 male and 11 female patients. The clinical presentation included seizures (n = 15), headache (n = 16), visual deficits (n = 7), cognitive disturbances (n = 3), and rhinorrhea (n = 1). Hyposmia was present in 14 cases, absent in 13 cases (39.3%), and unreported in five. Homogeneous and heterogeneous contrast enhancement was observed in 14 and 15 cases, respectively. The region of the olfactory groove was the probable site in 96.5%. Olfactory tract could be identified in 39.3%. The most probable origin is the meningeal branches of trigeminal nerve or anterior ethmoidal nerves. Thus, olfactory groove schwannoma would better describe its origin and pathogenesis and should be the term preferentially used to name it.
我们系统地回顾了有关前颅窝神经鞘瘤的文献,以了解其发病机制,确定其起源,并规范术语。我们对MEDLINE、EMBASE和科学引文索引扩展版进行了文献检索;分析并列表了年龄、性别、临床表现、是否存在嗅觉减退、放射学特征和明显起源。神经纤维瘤病背景下的病例以及伴有颅内扩展的鼻神经鞘瘤不包括在内。年龄在14岁至63岁之间(平均 = 30.9岁)。有22例男性患者和11例女性患者。临床表现包括癫痫发作(n = 15)、头痛(n = 16)、视力障碍(n = 7)、认知障碍(n = 3)和鼻漏(n = 1)。14例存在嗅觉减退,13例不存在(39.3%),5例未报告。分别在14例和15例中观察到均匀和不均匀的对比增强。96.5%的病例中嗅沟区域可能是发病部位。39.3%的病例中可识别出嗅束。最可能的起源是三叉神经或筛前神经的脑膜支。因此,嗅沟神经鞘瘤能更好地描述其起源和发病机制,应优先使用该术语来命名。