Division of Neurology, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.
Lupus. 2010 May;19(6):748-52. doi: 10.1177/0961203309351539. Epub 2010 Feb 4.
A 13-year-old girl with a known diagnosis of systemic lupus erythematosus presented with seizures and psychosis. An electroencephalogram (EEG) revealed continuous, non-evolving periodic lateralized epileptiform discharges (PLEDs) in the left temporal region, which did not resolve with benzodiazepine. A magnetic resonance imaging (MRI) brain scan demonstrated a focal hyperintensity in the left medial temporal and left occipital lobes, left thalamus and bilateral cerebellar white matter, with evidence of vasculitis in the magnetic resonance angiography. Intravenous immunoglobulin was given because of failed steroid therapy, which resulted in a full resolution of clinical, EEG and MRI abnormalities. Lupus cerebritis should be considered as a possible aetiology in PLEDs, and immunoglobulin can be effective in neuropsychiatric lupus.
一位 13 岁女孩被诊断患有系统性红斑狼疮,出现癫痫发作和精神病。脑电图(EEG)显示左颞区持续、非进展性周期性偏侧癫痫样放电(PLEDs),苯二氮䓬类药物治疗无效。磁共振成像(MRI)脑扫描显示左内侧颞叶和左枕叶、左丘脑和双侧小脑白质有局灶性高信号,磁共振血管造影显示血管炎。由于类固醇治疗失败,给予静脉注射免疫球蛋白,导致临床、脑电图和 MRI 异常完全消退。狼疮性脑炎应被视为 PLEDs 的可能病因,免疫球蛋白对神经精神性狼疮可能有效。