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Bilateral Optic Pathway Ganglioglioma: The Fifth Case in the Literature

机译:双边视神经节神经胶质瘤:文学中的第五例

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摘要

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 dysplasticeoplastic 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. (C) 2015 S. Karger AG, Basel
机译:神经节神经胶质瘤是既包含神经胶质又包含神经元元素的混合肿瘤。视神经通路是神经节神经胶质瘤非常罕见的部位,文献报道少于23例。之前仅4例报道了整个视神经通路的双侧受累。由于其他病理实体(例如神经胶质瘤和颅咽神经瘤)的放射学表现相似,因此组织病理学诊断至关重要。我们报告了涉及两个光学通路的神经节神经胶质瘤病例。评估了一个12岁的患者,他们的视力下降了6个月。经过视野测试和放射学检查后,进行了显微外科活检程序。病理检查发现增生/神经节神经节细胞和神经胶质细胞瘤,诊断为世界卫生组织(WHO)1级神经节神经胶质瘤。计划为患者安排辅助放疗,以防止进展。 (C)2015 S.Karger AG,巴塞尔

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