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首页> 外文期刊>Child's nervous system: ChNS : official journal of the International Society for Pediatric Neurosurgery >A rare case of a pediatric extraventricular neurocytoma: case report and review of the literature.
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A rare case of a pediatric extraventricular neurocytoma: case report and review of the literature.

机译:小儿室外神经细胞瘤的罕见病例:病例报告和文献复习。

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摘要

Central neurocytomas are well-demarcated, intraventricular tumors that display neuronal differentiation. Fifty percent of these lesions are located in the frontal horn or the body of the lateral ventricle near the foramen of Monro [2]. Extra-ventricular central neurocytoma refers to a rare parenchymal tumor with neurocytoma features. These tumors tend to be large, well-circumscribed lesions located in the cerebral hemispheres, most commonly in the frontal and parietal lobes, although they have been found in the thalamus, cerebellum, pineal region, and even in the spinal cord [15]. Although no consistent chromosomal gains or losses have been seen, 1p19q co-deletions have been found. This finding does not seem to imply a more favorable prognosis as with oligodendrogliomas [10, 13].
机译:中枢神经细胞瘤是界限分明的,显示神经元分化的脑室内肿瘤。这些病变的百分之五十位于门罗的额角或侧脑室的身体附近[2]。心室中枢神经细胞瘤是指一种罕见的具有神经细胞瘤特征的实质性肿瘤。尽管已在丘脑,小脑,松果体区域甚至在脊髓中发现,但这些肿瘤往往位于大脑半球,通常位于额叶和顶叶中,是大的,界限清楚的病变[15]。尽管没有观察到一致的染色体增益或损失,但已发现1p19q共缺失。这一发现似乎并不意味着比少突胶质细胞瘤更有利的预后[10,13]。

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