Subacute sclerosing panencephalitis with parkinsonian features in a child: A case report

被引:9
作者
Bozlu, Gulcin [1 ]
Direk, Meltem Cobanogullari
Okuyaz, Cetin
机构
[1] Mersin Univ, Fac Med, Dept Pediat, Mersin, Turkey
关键词
SSPE; Children; Atypical; Parkinsonism; SSPE;
D O I
10.1016/j.braindev.2015.02.008
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Subacute sclerosing panencephalitis (SSPE) can present with atypical clinical signs which may result in delayed diagnosis and treatment. We present a child with SSPE whose initial manifestation was parkinsonism. Patient: This 12-year-old boy presented with the complaint of difficulty in standing up and walking for 2 months. Neurological examination revealed generalized rigidity, bradykinesia, impaired postural reflexes, and a mask-like facies. The initial diagnosis of Juvenile Parkinson Disease was made. He had no improvement with levodopa, trihexyphenidyl, tetrabenazine and clonazepam. The EEG showed irregular background activity with generalized slow waves which were not suppressed with diazepam injection. SSPE was considered and the diagnosis was confirmed with the identification of measles antibodies in cerebrospinal fluid. Conclusion: SSPE should be considered in children and adolescents with parkinsonian symptoms, particularly in the absence of a history of vaccination against measles. (C) 2015 The Japanese Society of Child Neurology. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:901 / 903
页数:3
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