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首页> 外文期刊>Child's nervous system: ChNS : official journal of the International Society for Pediatric Neurosurgery >Pediatric giant cell glioblastoma: a case report and review of the literature.
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Pediatric giant cell glioblastoma: a case report and review of the literature.

机译:小儿巨细胞胶质母细胞瘤:一例报道并文献复习。

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INTRODUCTION: Giant cell glioblastoma is a subtype of glioblastoma multiforme (GM) whose most characteristic histology is the presence of plentiful multinucleated giant cells. These tumours are very rare and account for only 5% of GM. They do not have specific localization, although normally they are supratentorial and affect mostly the temporal lobe. They may occur at any age, but mostly they occur in younger people than GM. They are infrequent in childhood, but they have longer survival in paediatric age. CASE REPORT: We present an 11-year-old girl that was operated but whose tumour recurred in a month after apparent total removal. DISCUSSION: We review in the literature the clinical, histological, immuno-histochemical and genetic characteristics, as well the prognosis of this tumour.
机译:简介:巨细胞胶质母细胞瘤是多形胶质母细胞瘤(GM)的亚型,其最典型的组织学是大量多核巨细胞的存在。这些肿瘤非常罕见,仅占GM的5%。它们没有特定的定位,尽管通常它们是幕上的并且主要影响颞叶。它们可能发生在任何年龄,但大多数发生在比GM的年轻人中。他们在儿童时期很少见,但在儿童时期生存期更长。病例报告:我们介绍了一个11岁的女孩,该女孩已经手术,但在完全切除后一个月内肿瘤复发。讨论:我们在文献中回顾了该肿瘤的临床,组织学,免疫组织化学和遗传学特征以及其预后。

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