Karaaslan Burak, Uçar Murat, Kulduk Gamze, Börcek Alp Özgün, Baykaner M Kemali
Division of Pediatric Neurosurgery, Gazi University Faculty of Medicine, Ankara, Turkey.
Pediatr Neurosurg. 2016;51(1):48-54. doi: 10.1159/000439541. Epub 2015 Oct 22.
Gangliogliomas are mixed tumors which contain both glial and neuronal elements. The optic pathway is a very rare location for gangliogliomas, with less than 23 cases reported in the literature. Bilateral involvement of the entire optic pathway was reported in only 4 cases before. Because of similar radiological appearance of other pathological entities such as gliomas and craniopharyngiomas, histopathological diagnosis is essential. We report a ganglioglioma case that involved both optic pathways. A 12-year-old patient suffering from visual deterioration for 6 months was evaluated. After a visual field test and radiological examinations, a microsurgical biopsy procedure was performed. Pathological examination revealed dysplastic/neoplastic ganglion cells and neoplastic glial cells, and the diagnosis was a World Health Organization (WHO) grade 1 ganglioglioma. The patient is scheduled for adjuvant radiotherapy with the hope of prevention of progression.
节细胞胶质瘤是一种同时包含神经胶质和神经元成分的混合性肿瘤。视路是节细胞胶质瘤非常罕见的发病部位,文献报道不足23例。此前仅有4例报告累及双侧整个视路。由于胶质瘤和颅咽管瘤等其他病理实体具有相似的影像学表现,组织病理学诊断至关重要。我们报告1例累及双侧视路的节细胞胶质瘤病例。对一名视力减退6个月的12岁患者进行了评估。经过视野检查和影像学检查后,实施了显微手术活检。病理检查发现发育异常/肿瘤性神经节细胞和肿瘤性胶质细胞,诊断为世界卫生组织(WHO)1级节细胞胶质瘤。该患者计划接受辅助放疗,以期预防病情进展。