• 摘要: 眼阵挛-肌阵挛-共济失调综合征(OMAS)是一种罕见的神经系统疾病。该病常与神经母细胞瘤(NB)相关,我国儿童OMAS和NB分别由神经内科和肿瘤内、外科单独进行诊治。本组患儿中,NB通常预后良好,而OMAS易留有后遗症,但由于缺乏规范的诊治及随访,不利于患者疾病的控制。本文由多学科领域专家共同制订儿童NB相关性OMAS诊疗建议,从疾病的诊断、治疗、随访等方面进行阐述,希望通过对本组患儿的规范管理,改善患儿的预后。

     

    Abstract: Opsoclonus-myoclonus-ataxia syndrome(OMAS) is a rare neurological disorder. This disease is often associated with neuroblastoma(NB). OMAS and neuroblastoma in children in China are treated separately by neurology, medical and surgical oncology. In this group of children, NB usually has a good prognosis, while OMAS is prone to sequelae, but the lack of standardized evaluation and follow-up is not conducive to the diagnosis and treatment of the disease. In this study, experts from multidisciplinary fields worked together to develop recommendations for the diagnosis, treatment and follow-up of NB associated OMAS in children, hoping to improve the prognosis of children through standardized management of this group of children.

     

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