Department of Neurosurgery, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, No.56 Nanlishilu, West District, Beijing, 100045, China.
Childs Nerv Syst. 2024 May;40(5):1349-1360. doi: 10.1007/s00381-024-06280-4. Epub 2024 Jan 16.
To investigate the treatment plan and prognosis of children with ocular dyskinesia and hemifacial spasm secondary to pontine tumours adjacent to the fourth ventricle.
In this retrospective study, the clinical information of 10 consecutively collected children with ocular dyskinesia and hemifacial spasm secondary to pontine tumours adjacent to the fourth ventricle was analyzed. All 10 children underwent pontine tumour resection through a trans-cerebellomedullary fissure approach; 4 children underwent preoperative diffusion tensor imaging scans to determine the relationship between the tumour and facial nerve nucleus, and the other 6 children underwent intraoperative deep electroencephalography (EEG) tumour monitoring, in which the tumour electrical discharge activity of the tumour was recorded. A voxel distribution map was established to describe the distribution of the tumour location, and patient prognosis was evaluated through clinical and imaging follow-up.
All 10 children achieved total tumour resection; 9 tumours were pathologically suggested to be ganglioglioma (WHO grade I), and 1 was a hamartoma. The symptoms of the original ocular dyskinesia and hemifacial spasm disappeared immediately after the operation. The children were followed up for 4-75 months, and none of the symptoms recurred; four cases with preoperative diffusion tensor imaging showed that the tumour was close to the facial nerve. Four in six intraoperative electrophysiological monitoring showed that the tumour had electrical discharge behaviour, and the tumour distribution map indicates a high density of tumour presence in the facial nerve nucleus and the nucleus of the abducens nerve.
In paediatric patients, the facial symptoms are related to the location and abnormal electrical discharge of the tumour. There is no significant correlation between ocular dyskinesia and the location of the tumour. Conventional antiepileptic therapy for this disease is ineffective, and early surgical intervention for total tumour resection can achieve a clinical curative effect.
探讨桥脑第四脑室旁肿瘤继发眼动障碍和面肌痉挛的治疗方案及预后。
回顾性分析 10 例桥脑第四脑室旁肿瘤继发眼动障碍和面肌痉挛患儿的临床资料。10 例患儿均经小脑延髓裂入路行桥脑肿瘤切除术,4 例行术前弥散张量成像扫描,以明确肿瘤与面神经核的关系,6 例行术中深部脑电图(EEG)肿瘤监测,记录肿瘤电活动。建立肿瘤位置分布的体素分布图,通过临床和影像学随访评估患者预后。
10 例患儿均达到肿瘤全切除,9 例肿瘤病理提示为神经节细胞瘤(WHO Ⅰ级),1 例为错构瘤。术后原有的眼动障碍和面肌痉挛症状立即消失。10 例患儿随访 4~75 个月,均无症状复发,4 例术前弥散张量成像显示肿瘤与面神经接近。6 例术中电生理监测中有 4 例显示肿瘤有放电行为,肿瘤分布图显示面神经核和展神经核有高密度肿瘤存在。
在儿童患者中,面部症状与肿瘤的位置和异常放电有关,眼动障碍与肿瘤位置无明显相关性。该疾病的常规抗癫痫治疗无效,早期行肿瘤全切除的手术干预可获得良好的临床疗效。