Opsoclonus/myoclonus: paraneoplastic syndrome of neuroblastoma.
作者信息
Janss A, Sladky J, Chatten J, Johnson J
机构信息
Department of Neurology, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, USA.
出版信息
Med Pediatr Oncol. 1996 Apr;26(4):272-9. doi: 10.1002/(SICI)1096-911X(199604)26:4<272::AID-MPO11>3.0.CO;2-H.
Abstract
摘要
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Opsoclonus/myoclonus: paraneoplastic syndrome of neuroblastoma.眼阵挛/肌阵挛：神经母细胞瘤的副肿瘤综合征。
Med Pediatr Oncol. 1996 Apr;26(4):272-9. doi: 10.1002/(SICI)1096-911X(199604)26:4<272::AID-MPO11>3.0.CO;2-H.
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Late detection of neuroblastoma in a patient with prolonged cerebellar ataxia without opsoclonus.一名患有持续性小脑共济失调且无眼阵挛的患者神经母细胞瘤的晚期检测。
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Long-term neurologic outcome in children with opsoclonus-myoclonus associated with neuroblastoma: a report from the Pediatric Oncology Group.与神经母细胞瘤相关的眼阵挛-肌阵挛患儿的长期神经学转归：来自儿童肿瘤协作组的报告
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引用本文的文献
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Comparison of mediastinal and non-mediastinal neuroblastoma and ganglioneuroblastoma associated with opsoclonus-myoclonus syndrome: a systematic review and meta-analysis.与眼阵挛-肌阵挛综合征相关的纵隔和非纵隔神经母细胞瘤及神经节神经母细胞瘤的比较：一项系统评价和荟萃分析
Transl Cancer Res. 2022 Oct;11(10):3741-3753. doi: 10.21037/tcr-22-1120.
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Neuroblastic tumors associated with opsoclonus-myoclonus syndrome: histological, immunohistochemical and molecular features of 15 Italian cases.与眼阵挛-肌阵挛综合征相关的神经母细胞瘤：15例意大利病例的组织学、免疫组化及分子特征
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