Department of Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, Tiantan Xili 6, Dongcheng District, Beijing City, 100050, China.
Acta Neurochir (Wien). 2013 Jul;155(7):1253-60. doi: 10.1007/s00701-013-1728-7. Epub 2013 May 3.
Ganglioglioma is mostly found in cerebral parenchymal, and it is rarely located in the ventricular system. To date, ganglioglioma within the ventricular system has been reported in only 10 cases. Its prognosis and relationship with complicating hydrocephalus are unclear.
A total of 7 cases with intraventricular ganglioglioma diagnosed by the surgical pathology examination from June 2004 to April 2011 in our center were retrospectively analyzed. The clinical data were collected from the clinical medical records, and the tumor site, size and basement of tumor were analyzed. Follow up was performed to obtain the clinical outcomes.
The 7 cases included 5 males and 2 females, with disease onset at 23.6 ± 14.9 years old. Epilepsy as the initial symptom was observed in 1 case. Reduced hearing, dizziness and weakness of both lower limbs were found in 1 case. Intracranial hypertension were detected in 5 cases, including 1 case complicating by decreased visual acuity. Tumors were located in the lateral ventricle in 5 cases, while 2 cases in the third ventricle. Hydrocephalus was observed in 5 cases, including 2 cases with severe hydrocephalus, and both underwent ventriculoperitoneal shunting. Total resection of tumors was performed in 5 cases, and 2 cases underwent gross total resection. The mean duration of follow-up was 28.7 months (8-90 months). Intracranial hypertension in all cases disappeared. Even radiotherapy post-surgery, one case with GTR relapsed 1 year later. However, the other 6 cases didn't relapse.
Ganglioglioma in ventricular system is extremely rare, mainly with the symptoms of intracranial hypertension or seizure. The degree of hydrocephalus is closely related to the site of tumor's basement. The prognosis is good after total resection. The patients with GTR should be followed-up.
神经节细胞瘤主要发生在脑实质,而发生在脑室系统的情况很少见。迄今为止,脑室系统内的神经节细胞瘤仅在 10 例中报道过。其预后和与并发脑积水的关系尚不清楚。
回顾性分析 2004 年 6 月至 2011 年 4 月我中心通过手术病理检查诊断的 7 例脑室神经节细胞瘤患者。收集临床病历中的临床资料,分析肿瘤部位、大小及肿瘤基底。进行随访以获得临床结果。
7 例患者中男 5 例,女 2 例,发病年龄为 23.6±14.9 岁。1 例以癫痫为首发症状。1 例出现听力下降、头晕、双下肢无力。5 例颅内压升高,其中 1 例伴有视力下降。肿瘤位于侧脑室 5 例,第三脑室 2 例。脑积水 5 例,其中 2 例为重度脑积水,均行脑室-腹腔分流术。肿瘤全切除 5 例,大体全切除 2 例。平均随访时间为 28.7 个月(8-90 个月)。所有病例颅内压升高均消失。即使术后放疗,1 例 GTR 复发 1 年后。但其余 6 例没有复发。
脑室系统神经节细胞瘤极为罕见,主要表现为颅内压增高或癫痫。脑积水的程度与肿瘤基底的部位密切相关。完全切除后预后良好。GTR 患者应进行随访。