Gebremariam A, Lulseged S, Tamrat A
Department of Paediatrics and Child Health, Ethio-Swedish Children's Hospital, Addis Ababa, Ethiopia.
Ann Trop Paediatr. 1987 Dec;7(4):262-3. doi: 10.1080/02724936.1987.11748521.
Some 50 years have elapsed since Dawson first described a 16-year-old girl with an inclusion encephalitis. Since then, numerous publications on subacute sclerosing panencephalitis (SSPE) have appeared in the world literature. However, most of these reports are from the developed world. There have been few reports from Africa. One of them was from Kenya, where a retrospective analysis of EEGs of patients with epilepsy over a 5-year period identified 53 probable cases of subacute sclerosing panencephalitis (1). The other one was from South Africa where an incidence of 1.2 per million per year was reported on the basis of 15 cases collected from two hospitals in the Cape Province (2). No case, as yet, has been reported from Ethiopia. This paper reports SSPE presenting in an adolescent Ethiopian girl who had measles at the age of 18 months.
自道森首次描述一名患有包涵体脑炎的16岁女孩以来,已经过去了大约50年。从那时起,世界文献中出现了大量关于亚急性硬化性全脑炎(SSPE)的出版物。然而,这些报告大多来自发达国家。来自非洲的报告很少。其中一份来自肯尼亚,在那里对5年内癫痫患者的脑电图进行回顾性分析,确定了53例可能的亚急性硬化性全脑炎病例(1)。另一份来自南非,根据从开普省两家医院收集的15例病例报告,每年的发病率为百万分之一(2)。埃塞俄比亚尚未报告过病例。本文报告了一名18个月大时患过麻疹的埃塞俄比亚青少年女孩出现亚急性硬化性全脑炎的情况。