Marutirao Raghavendra, Singh Suyash, Bhasiora Kamlesh Singh, Pandey Satyadeo, Sardhara Jayesh, Das Kuntal Kanti, Srivastava Arun Kumar, Jaiswal Sushila, Behari Sanjay
Department of Neurosurgery, SGPGIMS, Lucknow, Uttar Pradesh, India.
Department of Pathology, SGPGIMS, Lucknow, Uttar Pradesh, India.
Asian J Neurosurg. 2018 Oct-Dec;13(4):1269-1272. doi: 10.4103/ajns.AJNS_104_18.
Cranial nerve schwannomas usually arise from sensory nerve and the occurrence of schwannoma in a motor nerve is rare, especially in sporadic cases. Oculomotor nerve schwannomas (ONS) are rare and they are unique as they arise from motor nerve. ONS palsy may or may not be the presenting feature of oculomotor schwannoma. We present the case of a young male with ONS, presenting with oculomotor nerve palsy along with features of raised intracranial pressure. Oculomotor schwannoma is described in literature only as case reports, and oculomotor nerve is also a rare site for schwannoma as being a motor nerve. In this article, we describe a case of cisternal ONS with review of pertinent literature.
颅神经鞘瘤通常起源于感觉神经,而运动神经发生鞘瘤较为罕见,尤其是在散发病例中。动眼神经鞘瘤(ONS)罕见,且因其起源于运动神经而独具特点。ONS麻痹可能是动眼神经鞘瘤的首发症状,也可能不是。我们报告一例年轻男性ONS病例,该患者表现为动眼神经麻痹及颅内压升高的症状。文献中关于动眼神经鞘瘤的描述仅为病例报告,而且动眼神经作为运动神经,也是鞘瘤的罕见发病部位。在本文中,我们描述一例脑池内ONS病例并对相关文献进行综述。