Department of Neurological Surgery, Indiana University School of Medicine, Indianapolis, Indiana, USA.
MD Degree Program, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Neuropathology. 2024 Dec;44(6):440-444. doi: 10.1111/neup.12996. Epub 2024 Jul 28.
The 2021 World Health Organization (WHO) classification of the central nervous system (CNS) tumors has classified diffuse leptomeningeal glioneuronal tumor (DLGNT) as a mixed neuronal and glial tumor. Here, we report a DLGNT with two distinct morphological tumor components but identical molecular features. A four-year-old female child presented with progressive right upper extremity weakness. Magnetic resonance imaging (MRI) revealed the leptomeningeal enhancement over the brain stem and cervicothoracic spine. The histological examination of surgical specimens revealed two distinct tumor components: approximately half of the tumor is composed of oligodendroglioma-like tumor intermingled with nodules of ganglioglioma-like tumor. Immunohistochemistry confirmed the oligodendroglioma and ganglioglioma features. The molecular genetic studies demonstrated the features of DLGNT, including fusion of KIAA1549::BRAF, deletion of chromosome 1p, and absence of isocitrate dehydrogenase 1/2 (IDH1/2) mutation in both tumor components. Interestingly, the genetic studies also revealed the distinct chromosomal abnormalities of the loss of chromosome 4 only in oligodendroglioma-like tumor and copy neutral loss of heterozygosity of 7Q34Q36.3 in the ganglioglioma-like tumor component. This case highlights the critical role of molecular testing in the diagnosis of rare cases of DLGNT with diverse morphological components as well as in the identification of unique molecular alternations responsible for morphological phenotypes of the distinct tumors in DLGNT.
2021 年世界卫生组织(WHO)中枢神经系统(CNS)肿瘤分类将弥漫性软脑膜胶质神经元肿瘤(DLGNT)归类为混合性神经元和神经胶质肿瘤。在此,我们报告了一例具有两种截然不同形态学肿瘤成分但具有相同分子特征的 DLGNT。一名 4 岁女性患儿出现进行性右上肢无力。磁共振成像(MRI)显示脑干和颈胸段软脑膜增强。手术标本的组织学检查显示出两种截然不同的肿瘤成分:大约一半的肿瘤由少突胶质细胞瘤样肿瘤与神经节细胞瘤样肿瘤结节混合而成。免疫组织化学证实了少突胶质细胞瘤和神经节细胞瘤的特征。分子遗传学研究显示了 DLGNT 的特征,包括 KIAA1549::BRAF 融合、1p 染色体缺失以及两种肿瘤成分中均不存在异柠檬酸脱氢酶 1/2(IDH1/2)突变。有趣的是,遗传研究还揭示了两种不同的染色体异常,即仅在少突胶质细胞瘤样肿瘤中丢失染色体 4,以及在神经节细胞瘤样肿瘤成分中存在 7Q34Q36.3 的拷贝中性杂合性丢失。本病例强调了分子检测在诊断具有不同形态成分的罕见 DLGNT 病例以及鉴定导致 DLGNT 中不同肿瘤形态表型的独特分子改变方面的重要作用。