Kansu T, Ozcan O E, Ozdirim E, Onol B, Gürcay O
J Clin Neuroophthalmol. 1982 Dec;2(4):271-2.
A 15-year-old boy with a recurrent third nerve palsy who was found to have a neurinoma of the third nerve is described. Unusual features of his presentation and review of the literature relative to this rare tumor are discussed. Tumors derived from Schwann cells, which wrap around the axons of peripheral nerves, are called neurinomas, neurofibromas, plexiform neurofibromas, neurilemomas, and schwannomas. Neurinomas are usually localized in the peripheral nerves. The most frequent site of occurrence of an intracranial schwannoma is the acoustic nerve; however, the tumor may occur along the second, fifth, seventh, 11th, and 12th cranial nerves. Neurinomas of the oculomotor nerves are extremely rare. In the literature, there are only four reported cases clinically manifested and pathologically verified as neurinomas of the third nerve.
本文描述了一名15岁复发性动眼神经麻痹男孩,其被发现患有动眼神经神经鞘瘤。讨论了该病例不寻常的临床表现以及相对于这种罕见肿瘤的文献综述。源自包裹周围神经轴突的施万细胞的肿瘤,被称为神经鞘瘤、神经纤维瘤、丛状神经纤维瘤、神经膜瘤和施万细胞瘤。神经鞘瘤通常位于周围神经。颅内施万细胞瘤最常见的发生部位是听神经;然而,该肿瘤也可能沿着第二、第五、第七、第十一和第十二对脑神经发生。动眼神经神经鞘瘤极为罕见。在文献中,仅有4例经临床证实且病理确诊为动眼神经神经鞘瘤的病例报道。