Almubarak Abdulaziz O, Abdullah Jamal, Al Hindi Hindi, AlShail Essam
Department of Neuroscience, King Faisal Specialist Hospital and Research Center, Riyadh, Kingdom of Saudi Arabia. E-mail:
Neurosciences (Riyadh). 2020 Jan;25(1):61-64. doi: 10.17712/nsj.2020.1.20190044.
Subependymal giant cell astrocytoma is a benign WHO grade I intraventricular tumor arise in patients with tuberous sclerosis complex. Previous reported described histopathological predictors of more aggressive forms, terms atypical SEGA in infantile age group. Other reports showed possible transformation of SEGA into glioblastoma, or misdiagnosis as glioblastoma due to the presence of atypical histopathological features. Here, we report a case of an infant who presented with right frontal extraventricular SEGA and underwent craniotomy with complete resection. Eight months later, he presented with fast recurrence in same location with midline shift and subfalcine herniation. Histopathological description showed high grade features including Ki labeling index of 60%, atypical mitotic figures, cellular plemorphism and necrosis. We also discussed the possible presence of different entity (termed atypical SEGA) which may have more aggressive clinical course, with literature review of predictors of SEGA aggressiveness and possible transformation/misdiagnosis as glioblastoma.
室管膜下巨细胞星形细胞瘤是一种WHO I级良性脑室内肿瘤,发生于结节性硬化症患者。既往报道描述了更具侵袭性形式的组织病理学预测指标,在婴儿年龄组中称为非典型室管膜下巨细胞星形细胞瘤。其他报道显示室管膜下巨细胞星形细胞瘤可能转化为胶质母细胞瘤,或因存在非典型组织病理学特征而被误诊为胶质母细胞瘤。在此,我们报告一例婴儿,其表现为右侧额叶脑室外室管膜下巨细胞星形细胞瘤并接受了开颅全切术。八个月后,他在同一部位快速复发,伴有中线移位和大脑镰下疝。组织病理学描述显示具有高级别特征,包括Ki标记指数为60%、非典型有丝分裂象、细胞多形性和坏死。我们还讨论了可能存在不同实体(称为非典型室管膜下巨细胞星形细胞瘤),其临床病程可能更具侵袭性,并对室管膜下巨细胞星形细胞瘤侵袭性的预测指标以及可能转化/误诊为胶质母细胞瘤进行了文献综述。