Department of Neurosurgery, Institute of Neurosciences, Apollo Speciality Hospitals, Apollo Proton Cancer Centre, Chennai, India.
Department of Neurosurgery, Institute of Neurosciences, Apollo Speciality Hospitals, Apollo Proton Cancer Centre, Chennai, India.
World Neurosurg. 2021 Feb;146:261-269. doi: 10.1016/j.wneu.2020.10.023. Epub 2020 Nov 5.
Glioblastomas (World Health Organization grade IV) are aggressive primary neoplasms of the central nervous system. Spinal metastasis occurs supposedly in 2%-5% of patients. This percentage may be only the tip of iceberg because most succumb to the disease before clinical detection and few documented cases are reported.
A 45-year-old man presented with history of diplopia and gait disturbance. Magnetic resonance imaging showed a left cerebellar space-occupying lesion. The histopathology was consistent with glioblastoma. The patient underwent adjuvant chemoradiation. A year later, he presented with seizures, worsening headache, neck stiffness, and low back pain. Imaging showed metastasis to the S1/S2 region of the spinal canal. A 29-year-old man presented with episodic headaches associated with nausea, vomiting, neck stiffness, and imbalance while walking. Computed tomography of the brain showed a hypodense lesion involving the left midbrain, pons, and left middle cerebellar peduncle, causing fourth ventricular pressure with obstructive hydrocephalus. A navigation-guided biopsy of the brainstem lesion confirmed the diagnosis of glioblastoma World Health Organization grade IV, isocitrate dehydrogenase 1 (R132 H) and H3K27M negative. Isocitrate dehydrogenase gene sequencing was suggested. The patient was referred for chemoradiation. During treatment, he worsened neurologically and developed axial neck and back pain. Neuraxis screening showed disseminated leptomeningeal spread, which was confirmed on dural biopsy.
Spinal and dural metastasis should always be suspected in patients with glioblastoma with signs and symptoms not explained by primary lesion. A regular protocol with postcontrast magnetic resonance imaging before and after initial surgery is mandatory to detect spinal metastasis before it becomes clinically apparent, thereby improving the prognosis and quality of life in patients.
胶质母细胞瘤(世界卫生组织四级)是一种侵袭性的中枢神经系统原发性肿瘤。据推测,脊髓转移发生在 2%-5%的患者中。这个百分比可能只是冰山一角,因为大多数患者在临床检测前就已死亡,而且很少有记录在案的病例报告。
一名 45 岁男性,出现复视和步态不稳的病史。磁共振成像显示左侧小脑占位性病变。组织病理学检查结果与胶质母细胞瘤一致。患者接受了辅助放化疗。一年后,他出现癫痫发作、头痛加剧、颈部僵硬和下腰痛。影像学检查显示椎管内转移至 S1/S2 节段。一名 29 岁男性,出现阵发性头痛,伴有恶心、呕吐、颈部僵硬和行走时失去平衡。脑 CT 显示左中脑、脑桥和左侧小脑脚的低密度病变,导致第四脑室受压和梗阻性脑积水。导航引导下的脑干病变活检证实了胶质母细胞瘤四级、异柠檬酸脱氢酶 1(R132H)和 H3K27M 阴性的诊断。建议进行异柠檬酸脱氢酶基因测序。该患者被转介接受放化疗。在治疗过程中,他的神经功能恶化,出现颈部和背部轴向疼痛。中枢神经系统筛查显示弥漫性软脑膜播散,硬脑膜活检证实了这一点。
对于有症状且无法用原发性病变解释的胶质母细胞瘤患者,应始终怀疑存在脊髓和硬脑膜转移。在初始手术后,必须常规进行增强磁共振成像检查,以在脊髓转移变得临床明显之前发现它,从而改善患者的预后和生活质量。