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小脑共济失调和眼球阵挛作为神经母细胞瘤相关肌阵挛性脑病的初始表现。

Cerebellar ataxia and opsoclonus as the initial manifestations of myoclonic encephalopathy associated with neuroblastoma.

作者信息

Harel S, Yurgenson U, Rechavi G, Burstein Y, Spirer Z

机构信息

Pediatric Neurology Unit, Tel Aviv Medical Center, Sackler Medical School, University of Tel Aviv, Israel.

出版信息

Childs Nerv Syst. 1987;3(4):245-7. doi: 10.1007/BF00274060.

Abstract

Cerebellar ataxia and opsoclonus were the initial manifestations of an associated neuroblastoma in a 20-month-old girl. Two months after the initial symptomatology, a physical examination revealed an abnormal mass palpable left to the midline. Urinary catecholamines were within normal limits. The child's neurological findings improved immediately after surgery, and steroid treatment and the follow-up on her after 2 years revealed normal general and neurological development. The syndrome of myoclonic encephalopathy including cerebellar ataxia, myoclonus and opsoclonus, and its relationship to neuroblastoma is reviewed. Failure to recognize this association can result in delays in both diagnosis and treatment and could be fatal.

摘要

一名20个月大女孩的小脑共济失调和眼阵挛是相关神经母细胞瘤的初始表现。最初出现症状两个月后,体格检查发现中线左侧可触及异常肿块。尿儿茶酚胺在正常范围内。手术后患儿的神经学检查结果立即改善,类固醇治疗及2年后的随访显示其全身和神经发育正常。本文综述了包括小脑共济失调、肌阵挛和眼阵挛在内的肌阵挛性脑病综合征及其与神经母细胞瘤的关系。未能认识到这种关联可能导致诊断和治疗延迟,甚至可能是致命的。

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