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Subependymal Giant Cell Astrocytoma Presenting with Tumoral Bleeding: A Case Report

机译:室管膜下巨细胞星形细胞瘤伴肿瘤出血:一例报告

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摘要

We report a rare case of subependymal giant cell astrocytoma (SEGA) associated with tumoral bleeding in a pediatric patient without tuberous sclerosis complex (TSC). A 10-year-old girl presented with a 2-week history of an increasingly aggravating headache. Brain magnetic resonance imaging revealed an approximately 3.6-cm, well-defined, heterogeneously enhancing mass with multistage hemorrhages on the right-sided foramen of Monro. The tumor was completely resected using a transcallosal approach. Intraoperatively, the mass presented as a gray-colored firm tumor associated with acute and subacute hemorrhages. The origin of the mass was identified as the ventricular septum adjacent to the foramen of Monro. A pathological analysis revealed pleomorphic multinucleated eosinophilic tumor cells with abundant cytoplasm. These cells showed positive staining for the glial fibrillary acidic protein and S100 protein. A diagnosis of SEGA was established. The patient recovered without any neurological symptoms. There was no evidence of TSC. The radiological follow-up showed no recurrence for 2 years. This was a case of SEGA with intratumoral hemorrhage, for which a favorable outcome was achieved, without any neurological deficit after tumoral resection.
机译:我们报告了少见的表皮下巨细胞星形细胞瘤(SEGA)与没有结节性硬化症(TSC)的儿科患者的肿瘤出血相关的情况。一名10岁女孩有2周的头痛加剧史。脑磁共振成像显示,门罗右侧孔上有一个约3.6厘米的界限分明的异质性肿块,伴有多阶段出血。使用经愈创方法将肿瘤完全切除。术中,肿块呈灰色实性肿瘤,伴有急性和亚急性出血。肿块的起源被确定为邻近门罗孔的室间隔。病理分析显示多形性多核嗜酸性肿瘤细胞具有丰富的细胞质。这些细胞显示神经胶质原纤维酸性蛋白和S100蛋白染色阳性。建立了SEGA的诊断。病人康复无任何神经系统症状。没有TSC的证据。放射学随访显示2年无复发。这是一例SEGA伴有肿瘤内出血,取得了良好的效果,肿瘤切除后没有任何神经功能缺损。

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