Department of Pathology, Universidade Federal de São Paulo, Escola Paulista, de Medicina, São Paulo, Brazil; Laboratory of Molecular and Experimental Pathology, Universidade Federal, de São Paulo, Escola Paulista de Medicina, São Paulo, Brazil.
Department of Pathology, Universidade Federal de São Paulo, Escola Paulista, de Medicina, São Paulo, Brazil; Laboratory of Molecular and Experimental Pathology, Universidade Federal, de São Paulo, Escola Paulista de Medicina, São Paulo, Brazil.
Pathol Res Pract. 2023 Dec;252:154942. doi: 10.1016/j.prp.2023.154942. Epub 2023 Nov 14.
Pilocytic astrocytoma is the most common primary CNS neoplasm in children and adolescents, rare after the first two decades of life. While some authors report a favorable prognosis in the adult age group with the tumor, others have associated it with higher mortality. The molecular alteration most observed in cases of pilocytic astrocytoma in the pediatric group is the BRAF-KIAA1549 gene fusion, and there are still few studies confirming the presence of this fusion in the adult population. This work investigated genetic alterations involving the 7q34 region in BRAF gene in 21 adult individuals with pilocytic astrocytoma, by FISH. In addition, was identified the immunohistochemical expression of BRAFV600E, correlating these findings with histopathological and clinical ones. BRAF-KIAA1549 fusion appeared in only one case, while in two other cases were found deletions related to the FAM131B-BRAF fusion, suggesting that maybe the latter is more frequently in this population. Through the evaluation of immunoreactivity, 71% of the cases were considered positive and 29% negative. Cases considered positive for BRAFV600E immunoreactivity can potentially be treated through drug therapy with BRAF inhibitors; however, it is always recommended to carry out a molecular study for diagnostic confirmation. This is the first Brazilian study that aimed to investigate possible genetic alterations in the BRAF gene in pilocytic astrocytomas, specifically in adults. Only 1 patient died, but due to operative complications and not the disease itself, suggesting a good evolution of these individuals.
毛细胞型星形细胞瘤是儿童和青少年中最常见的原发性中枢神经系统肿瘤,在生命的头二十年之后很少见。虽然有些作者报告说肿瘤在成年人群中预后良好,但也有作者认为其与更高的死亡率相关。在儿科人群中观察到的毛细胞型星形细胞瘤中最常见的分子改变是 BRAF-KIAA1549 基因融合,而在成年人群中证实存在这种融合的研究仍然较少。这项工作通过 FISH 研究了 21 例成人毛细胞型星形细胞瘤中涉及 7q34 区域 BRAF 基因的遗传改变。此外,还鉴定了 BRAFV600E 的免疫组织化学表达,将这些发现与组织病理学和临床发现相关联。仅在一个病例中发现了 BRAF-KIAA1549 融合,而在另外两个病例中发现了与 FAM131B-BRAF 融合相关的缺失,这表明后者在该人群中可能更为常见。通过评估免疫反应性,71%的病例被认为是阳性,29%的病例是阴性。被认为具有 BRAFV600E 免疫反应性的病例可以通过 BRAF 抑制剂的药物治疗进行治疗;然而,总是建议进行分子研究以进行诊断确认。这是巴西第一项旨在研究毛细胞型星形细胞瘤中 BRAF 基因可能发生的遗传改变的研究,特别是在成年人中。只有 1 例患者死亡,但由于手术并发症而不是疾病本身,这表明这些患者的预后良好。