Tandra Harish Varma, Roy Pritam Singha, Sharma Rahul, Bhatia Vikas, Saini Arushi Gahlot
Pediatric Neurology and Neurodevelopment Unit, Department of Pediatrics, Advanced Pediatrics Centre, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Department of Radiodiagnosis, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Neurohospitalist. 2019 Jan;9(1):26-29. doi: 10.1177/1941874418776902. Epub 2018 May 16.
Subacute sclerosing panencephalitis is a devastating neurodegenerative disorder characterized by cognitive and memory deterioration, personality changes, behavior abnormalities, and a steady motor decline. Extrapyramidal manifestations are commonly seen in the advanced stage of the disease. We discuss a 10-year-old boy with subacute sclerosing panencephalitis presenting with generalized choreoathetosis, myoclonus, and cognitive decline. He had not been immunized for measles. His elder sister had a viral exanthematous illness 4 years ago. Magnetic resonance imaging revealed bilateral, asymmetric putaminal hyperintensities. A diagnosis of subacute sclerosing panencephalitis was confirmed by periodic complexes in the electroencephalograph and elevated antimeasles antibody titers in the blood and cerebrospinal fluid (1:625). Our case highlights that atypical clinical and radiological features of subacute sclerosing panencephalitis should always be borne in mind in children from endemic areas. Generalized choreoathetosis and bilateral putaminal involvement in the index case add to the spectrum of atypical presentations of subacute sclerosing panencephalitis in children.
亚急性硬化性全脑炎是一种毁灭性的神经退行性疾病,其特征为认知和记忆衰退、人格改变、行为异常以及运动功能持续下降。锥体外系表现常见于疾病晚期。我们讨论一名10岁患亚急性硬化性全脑炎的男孩,其表现为全身性舞蹈手足徐动症、肌阵挛和认知衰退。他未接种过麻疹疫苗。他的姐姐4年前患过病毒性疹病。磁共振成像显示双侧、不对称的壳核高信号。脑电图中的周期性复合波以及血液和脑脊液中抗麻疹抗体滴度升高(1:625)确诊为亚急性硬化性全脑炎。我们的病例强调,来自流行地区的儿童应始终牢记亚急性硬化性全脑炎的非典型临床和放射学特征。本例中的全身性舞蹈手足徐动症和双侧壳核受累增加了儿童亚急性硬化性全脑炎非典型表现的范围。