脑神经节胶质瘤1例

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引用次数: 0

摘要

神经节神经胶质瘤是一种少见的中枢神经系统良性肿瘤,通常位于颞叶的幕上。幕下定位,尤其是小脑,并不常见。它占所有中枢神经系统肿瘤的0.4% - 7.6%,占脑肿瘤的1.3%,仅占髓内肿瘤的1%。临床上,幕上GG引起癫痫,而幕下GG由于局部肿块效应和颅内压升高的迹象导致局灶性神经功能缺损。一种称为神经节胶质瘤(GG)的良性脑瘤有时可以在大脑中发现。我们在这篇文章中描述了一个不寻常的儿科两例幕上和幕下GG与脊髓定位。我们的病人患有头痛和癫痫。颅骨磁共振成像显示右小脑半球有一个巨大的囊肿和附壁结节,使第四脑室变平。毛细胞星形细胞瘤是基于临床和影像学细节的临时诊断。髓外硬脊膜内活检和免疫组化显示GG,虽然GG是一种罕见的肿瘤,但它应列入儿童小脑囊肿和实性成分的鉴别诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cerebral ganglioglioma: a case report
Ganglioglioma (GG) is a benign and rare tumor of the central nervous system, typically located supratentorially in the temporal lobe. Subtentorial localization, particularly in the cerebellum, is uncommon.It represents 0.4% to 7.6% of all central nervous system tumors, 1.3% of brain tumors, and only 1% of intramedullary tumors. Clinically, supratentorial GG causes epilepsy, while subtentorial GG leads to focal neurological deficits due to local mass effect and signs of increased intracranial pressure. A benign brain tumor, called a ganglioglioma (GG), can sometimes be found in the cerebrum. We describe an unusual pediatric two cases of supra and subtentorially GG with a spinal cord localisation in this article. Our patient suffered from headache and epilepsy. Magnetic resonance imaging of the skull revealed a giant cyst with a mural nodule in the right cerebellar hemisphere that flattened the fourth ventricle. Pilocytic astrocytoma was the provisional diagnosis on the basis of clinical and imaging details. After biopsy and immunohistochemistry of the extramedullary intra dural process revealed the presence of a GG. Although GG is an uncommon tumor, it should be included in the differential diagnosis of a cerebellar mass with cystic and solid components in children.
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