Elzomor Hossam, El Menawi Salma, Elawady Heba, Elkinaai Naglaa, Elshafie Maged, Refaat Amal, Ghareeb Hany, Fawzy Mohamed
Departments of Pediatric Oncology.
National Cancer Institute.
J Pediatr Hematol Oncol. 2023 Mar 1;45(2):e194-e199. doi: 10.1097/MPH.0000000000002466. Epub 2022 Apr 25.
Opsoclonous myoclonous ataxia syndrome (OMAS) is a rare primarily immune-mediated disease in children. The current study aim was to find out the patterns and outcome of OMAS associated with neuroblastoma (NBL) among Children's Cancer Hospital-Egypt patients. Data was reviewed for 15 eligible patients enrolled between 2007 and 2016. OMAS treatment included prednisolone and cyclophosphamide with/without intravenous immunoglobulin; NBL treatment was given according to risk-corresponding protocol. Patients' age ranged from 0.75 to 12 years at presentation with male/female: 1.1/1. Concurrent diagnosis of OMAS and NBL occurred in 6 patients (40%). OMAS preceded NBL within 0.25 to 2 years in 33%, while NBL preceded OMAS within 0.5 to 1.5 years in 27%. Full OMAS picture was present in 10/15 patients, while 20% presented with truncal ataxia and myoclonus, 1 with truncal ataxia and opsoclonus, and 1 had opsoclonus and myoclonus. Median time till improvement of manifestations was 5 months. The 5-year OMAS progression-free survival was 33.3%, where 10 patients needed second-line therapy due to relapse/progression of OMAS. The median time to progression was 28 months measured from OMAS diagnosis. All patients remained alive with NBL 5-year overall survival of 100% and event-free survival of 85.7% for. However, 73% of the patients showed late sequelae ranging from ocular to cognitive, behavioral and motor disorders; rarely seizures and hemolytic anemia.
眼阵挛-肌阵挛共济失调综合征(OMAS)是一种罕见的主要由免疫介导的儿童疾病。本研究的目的是找出埃及儿童癌症医院患者中与神经母细胞瘤(NBL)相关的OMAS的模式和结局。回顾了2007年至2016年期间登记的15例符合条件的患者的数据。OMAS的治疗包括泼尼松龙和环磷酰胺,可加用或不加用静脉注射免疫球蛋白;NBL的治疗根据风险对应方案进行。患者就诊时年龄在0.75至12岁之间,男女比例为1.1∶1。6例患者(40%)同时诊断为OMAS和NBL。33%的患者OMAS先于NBL出现,时间在0.25至2年之间,而27%的患者NBL先于OMAS出现,时间在0.5至1.5年之间。15例患者中有10例出现了完整的OMAS症状,20%的患者表现为躯干共济失调和肌阵挛,1例表现为躯干共济失调和眼阵挛,1例表现为眼阵挛和肌阵挛。症状改善的中位时间为5个月。OMAS的5年无进展生存率为百分之33.3,其中10例患者因OMAS复发/进展需要二线治疗。从OMAS诊断开始计算,进展的中位时间为28个月。所有患者均存活,NBL的5年总生存率为100%,无事件生存率为百分之85.7。然而,73%的患者出现了晚期后遗症,从眼部到认知、行为和运动障碍;很少有癫痫发作和溶血性贫血。