伴有启动子突变的脑膜瘤恶性转化:病例报告
Malignant Transformation of Meningioma With Promoter Mutation: A Case Report.
作者信息
Hong Yoontae, Han Nayoung, Gwak Ho-Shin
机构信息
Department of Neurosurgery, Seoul National University College of Medicine, Seoul, Korea.
Department of Pathology, National Cancer Center, Goyang, Korea.
出版信息
Brain Tumor Res Treat. 2024 Jul;12(3):192-199. doi: 10.14791/btrt.2024.0023.
High-grade meningiomas make up a relatively minor proportion of meningiomas, which are one of the most common types of primary intracranial tumors in adults. Though rare, a considerable portion of high-grade meningiomas arise from malignant transformation of benign meningiomas. The 2021 World Health Organization (WHO) classification criteria introduced molecular markers in the diagnosis and grading of central nervous system (CNS) tumors and assigned certain genomic mutations to grade 3 meningiomas. We report a case of a 54-year-old male patient who underwent stepwise malignant transformation of meningioma from WHO grade 1 to grade 3 within 10 years, during the course of five surgeries followed by adjuvant stereotactic radiosurgery and radiotherapy. We performed next-generation sequencing (NGS) on the most recent grade 3 meningioma specimen and found that it carried a telomerase reverse transcriptase promoter (p) mutation (c.-124C>T) in accordance with the 2021 WHO criteria for grade 3 meningiomas. We then retrospectively examined the previous grade 1 and 2 specimens and found them to have the same mutation. We reviewed the significance of molecular markers in the diagnosis of meningiomas, possible genetic alterations associated with their malignant transformation, and what measures could be taken to effectively manage meningiomas considering NGS findings.
高级别脑膜瘤在脑膜瘤中所占比例相对较小,而脑膜瘤是成人最常见的原发性颅内肿瘤类型之一。尽管罕见,但相当一部分高级别脑膜瘤由良性脑膜瘤恶变而来。2021年世界卫生组织(WHO)分类标准在中枢神经系统(CNS)肿瘤的诊断和分级中引入了分子标志物,并将某些基因组突变归为3级脑膜瘤。我们报告了一例54岁男性患者,在10年内经历了脑膜瘤从世界卫生组织1级到3级的逐步恶变,期间进行了五次手术,随后辅助立体定向放射外科和放射治疗。我们对最新的3级脑膜瘤标本进行了二代测序(NGS),发现其携带端粒酶逆转录酶启动子(p)突变(c.-124C>T),符合2021年WHO 3级脑膜瘤标准。然后我们回顾性检查了之前的1级和2级标本,发现它们也有相同的突变。我们探讨了分子标志物在脑膜瘤诊断中的意义、与其恶变相关的可能基因改变,以及根据NGS结果可采取哪些措施有效治疗脑膜瘤。