Department of Pathology, Kurume University School of Medicine, Kurume, Japan.
Department of Neurosurgery, Kurume University School of Medicine, Kurume, Japan.
Neuropathology. 2024 Apr;44(2):161-166. doi: 10.1111/neup.12946. Epub 2023 Oct 1.
We report a case of pediatric glioma with uncommon imaging, morphological, and genetic features. A one-year-old boy incidentally presented with a tumor in the fourth ventricle. The tumor was completely resected surgically and investigated pathologically. The mostly circumscribed tumor had piloid features but primitive and anaplastic histology, such as increasing cellularity and mitosis. The Ki-67 staining index was 25% at the hotspot. KIAA1549::BRAF fusion and KIAA1549 partial deletions were detected by direct PCR, supported by Sanger sequencing. To the best of our knowledge, this is the first report of a glioma with both deletion of KIAA1549 p.P1771_P1899 and fusion of KIAA1549::BRAF. The tumor could not be classified using DNA methylome analysis. The present tumor fell into the category of pilocytic astrocytoma with histological features of anaplasia (aPA). Further studies are needed to establish pediatric aPA.
我们报告一例具有罕见影像学、形态学和遗传学特征的小儿脑胶质瘤。一名一岁男孩偶然发现第四脑室肿瘤。肿瘤经手术完全切除并进行病理检查。肿瘤主要呈局限性生长,具有类胚芽特征,但具有原始和间变的组织学特征,如细胞增多和有丝分裂。热点区 Ki-67 染色指数为 25%。通过直接 PCR 检测到 KIAA1549::BRAF 融合和 KIAA1549 部分缺失,并通过 Sanger 测序得到支持。据我们所知,这是首例同时存在 KIAA1549 p.P1771_P1899 缺失和 KIAA1549::BRAF 融合的脑胶质瘤报告。该肿瘤无法通过 DNA 甲基组分析进行分类。目前的肿瘤归入具有间变组织学特征的毛细胞星形细胞瘤(aPA)类别。需要进一步研究来建立小儿 aPA。