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Spinal Cord Glioneuronal Tumor with Rosetted Neuropil-Like Islands in Pediatric Age Group

机译:儿科年龄段伴有Rosetted Neuropil像岛的脊髓神经胶质神经瘤

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摘要

Glioneuronal neoplasms are rare tumors. Recently, an unusual glioneuronal tumor histologically showing neuropil-like islands has been described. Here, we present such a tumor originating from spinal cord of a 14-year-old girl, who has scoliosis and urinary incontinence. Microscopically, the glial component was chiefly fibrillary astrocytic, punctuated by neuropil-like islands. Immunohistochemically, glial tissue was GFAP positive, and neuropil-like areas and big neurons were synaptophysin reactive. For astrocytic component Ki-67 proliferation index was 1% and p53 was immunonegative. This case is unique in that in the literature it is the second reported case in pediatric age group that is located at spinal cord.
机译:胶质神经瘤是罕见的肿瘤。最近,已经描述了一种不寻常的胶质神经胶质瘤,其在组织学上显示出神经纤维样岛。在这里,我们介绍了一种源自脊柱侧凸和尿失禁的14岁女孩脊髓的肿瘤。在显微镜下,神经胶质成分主要是纤维状星形胶质细胞,被神经绒毛状岛刺穿。免疫组织化学观察,神经胶质组织为GFAP阳性,神经纤维样区域和大神经元为突触素反应性。对于星形细胞成分,Ki-67增殖指数为1%,p53为免疫阴性。这种情况是独特的,因为在文献中这是小儿年龄组中第二例报告的病例,位于脊髓。

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