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首页> 外文期刊>European journal of pediatric surgery = Zeitschrift fur Kinderchirurgie >Early Detection and Treatment of Neuroblastic Tumor with Opsoclonus-Myoclonus Syndrome Improve Neurological Outcome: A Review of Five Cases at a Single Institution in Japan
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Early Detection and Treatment of Neuroblastic Tumor with Opsoclonus-Myoclonus Syndrome Improve Neurological Outcome: A Review of Five Cases at a Single Institution in Japan

机译:早期发现和治疗伴有视神经丛肌阵挛综合征的神经母细胞瘤可改善神经系统疾病:日本一所机构的五例病例的回顾

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摘要

IntroductionOpsoclonus-myoclonus syndrome (OMS) is a paraneoplastic neurological disorder associated with neuroblastic tumor (NT) in childhood. Half of patients have neurological sequelae after the neurological and oncological treatment. We reviewed the neurological and oncological outcomes of NT with OMS, and discussed whether the treatment of NT would contribute to improving the neurological prognosis.
机译:简介输卵管肌肌阵挛综合征(OMS)是儿童时期与神经母细胞瘤(NT)相关的副肿瘤性神经系统疾病。经过神经和肿瘤治疗后,一半的患者患有神经系统后遗症。我们回顾了OMS对NT的神经和肿瘤学结局,并讨论了NT的治疗是否有助于改善神经学预后。

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