Hoving Eelco W, Kros Johan M, Groninger Ellis, den Dunnen Wilfred F A
Departments of Neurosurgery, University Medical Center Groningen, Groningen, The Netherlands.
J Neurosurg Pediatr. 2008 Jan;1(1):95-8. doi: 10.3171/PED-08/01/095.
Desmoplastic infantile gangliogliomas (DIGs) are rare supratentorial tumors that arise in infancy. Despite the large size of these lesions, the prognosis is generally considered favorable after gross-total resection (GTR); however, in incidental cases tumor progression has been described. The authors report on a child harboring a DIG with a high-grade primitive cell population and glial differentiation. The progressive clinical course was determined by this cell component in spite of GTR and adjuvant chemotherapy. The significance of the presence of a high-grade primitive tumor component in the context of DIG is discussed.
促纤维增生性婴儿型神经节胶质瘤(DIGs)是发生于婴儿期的罕见幕上肿瘤。尽管这些病变体积较大,但大体全切(GTR)后一般认为预后良好;然而,在偶然情况下也有肿瘤进展的报道。作者报告了1例患有DIG且伴有高级别原始细胞群和胶质分化的儿童。尽管进行了GTR和辅助化疗,但该细胞成分决定了其临床病程呈进展性。本文讨论了在DIG背景下存在高级别原始肿瘤成分的意义。