Choi Hyunho, Park Sung-Hye, Kim Dong Gyu, Paek Sun Ha
Department of Neurosurgery, Cancer Research Institute, Ischemic/Hypoxic Disease Institute, Seoul National University College of Medicine, Seoul, Korea.
J Korean Neurosurg Soc. 2011 Oct;50(4):381-4. doi: 10.3340/jkns.2011.50.4.381. Epub 2011 Oct 31.
The authors report a case of atypical extraventricular neurocytoma (EVN) transformed from EVN which had been initially diagnosed as an oligodendroglioma 15 years ago. An 8-year-old boy underwent a surgical resection for a right frontal mass which was initially diagnosed as oligodendroglioma. When the tumor recurred 15 years later, a secondary operation was performed, followed by salvage gamma knife treatment. The recurrent tumor was diagnosed as an atypical EVN. The initial specimen was reviewed and immunohistochemistry revealed a strong positivity for synaptophysin. The diagnosis of the initial tumor was revised as an EVN. The patient maintained a stable disease state for 15 years after the first operation, and was followed up for one year without any complications or disease progression after the second operation. We diagnosed an atypical extraventricular neurocytoma transformed from EVN which had been initially diagnosed as an oligodendroglioma 15 years earlier. We emphasize that EVN should be included in the differential diagnosis of oligodendroglioma.
作者报告了一例非典型脑室外神经细胞瘤(EVN),其由15年前最初被诊断为少突胶质细胞瘤的EVN转化而来。一名8岁男孩因右侧额叶肿块接受了手术切除,该肿块最初被诊断为少突胶质细胞瘤。15年后肿瘤复发,进行了二次手术,随后进行了挽救性伽玛刀治疗。复发肿瘤被诊断为非典型EVN。对初始标本进行复查,免疫组化显示突触素呈强阳性。初始肿瘤的诊断修订为EVN。患者在首次手术后病情稳定15年,二次手术后随访一年,无任何并发症或疾病进展。我们诊断了一例由15年前最初被诊断为少突胶质细胞瘤的EVN转化而来的非典型脑室外神经细胞瘤。我们强调,EVN应纳入少突胶质细胞瘤的鉴别诊断。