Abstract
Among paraneoplastic neurologic disorders (PND), opsoclonus-myoclonus syndrome, so-called "dancing eye syndrome," is a rare disorder combining multivectorial eye movements, involuntary multifocal myoclonus, and cerebellar ataxia. Although several paraneoplastic antibodies against postsynaptic or cell-surface antigens have been reported, usually most patients are serum antibody negative. We report a 65-year-old patient with opsoclonus-myoclonus syndrome revealing a small-cell lung carcinoma. If serologic antineuronal anti-body screening was negative, autoantibodies against glutamic acid decarboxylase (anti-GAD) were positive. Despite the specific anticancer treatment and high dose corticosteroids, the patient developed a severe and progressive encephalopathy and died 10 days later. © 2014 S. Laroumagne et al.
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CITATION STYLE
Laroumagne, S., Elharrar, X., Coiffard, B., Plojoux, J., Dutau, H., Breen, D., & Astoul, P. (2014). “dancing eye syndrome” secondary to opsoclonus-myoclonus syndrome in small-cell lung cancer. Case Reports in Medicine, 2014. https://doi.org/10.1155/2014/545490
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