Cho Yong-Hwan, Sung Kyung-Su, Song Young-Jin, Kim Dae-Cheol, Choi Sunseob, Kim Ki-Uk
Brain Tumor Institute Medical Science Research Center, College of Medicine, Dong-A University, Busan, Korea. ; Department of Neurosurgery, College of Medicine, Dong-A University, Busan, Korea.
Brain Tumor Institute Medical Science Research Center, College of Medicine, Dong-A University, Busan, Korea. ; Department of Pathology, College of Medicine, Dong-A University, Busan, Korea.
Brain Tumor Res Treat. 2014 Apr;2(1):43-7. doi: 10.14791/btrt.2014.2.1.43. Epub 2014 Apr 29.
Schwannomas account for about 8% of intracranial tumors and 90% are vestibular schwannomas. Oculomotor schwannoma without neurofibromatosis is extremely rare. A 41-year-old female presented with complaints of blurred vision, and the neurologic examination revealed afferent pupillary defect and decreased visual acuity of the left side. Brain magnetic resonance image showed an extra axial mass in the left superior orbital fissure. The patient underwent major surgery via the fronto-temporal approach. The tumor originated from the oculomotor nerve and was subtotally removed under microscopic surgery. The pathological findings confirmed the tumor as a schwannoma. After surgery, ptosis and medial gaze limitation of the left eye was detected, but the symptoms improved gradually.
神经鞘瘤约占颅内肿瘤的8%,其中90%为前庭神经鞘瘤。无神经纤维瘤病的动眼神经鞘瘤极为罕见。一名41岁女性因视力模糊就诊,神经系统检查发现左侧传入性瞳孔障碍及视力下降。脑部磁共振成像显示左侧眶上裂有一轴外肿块。患者经额颞入路接受了大手术。肿瘤起源于动眼神经,在显微镜下手术次全切除。病理结果证实肿瘤为神经鞘瘤。术后发现左眼上睑下垂及内视受限,但症状逐渐改善。