Chronic periodic lateralised epileptic discharges and anti‐N‐methyl‐D‐aspartate receptor antibodies. Issue 2 (June 2014)

• Record Type: Journal Article
• Authors: Sakakibara, Eisuke; Takahashi, Yukitoshi; Murata, Yoshiko; Taniguchi, Go; Sone, Daichi; Watanabe, Masako
• Is Part Of: Epileptic disorders. Volume 16:Issue 2(2014:Jun.)
• Page Start: 218
• Page End: 222
• Publication Date: 2014-06
• Subjects: Epilepsy -- Periodicals; 616.853
• DOI: 10.1684/epd.2014.0655
• Languages: English
• ISSNs: 1294-9361

Abstract

<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Periodic lateralised epileptiform discharges (PLEDs) are uncommon transient electroencephalographic findings accompanied by acute brain lesions. A small proportion of PLEDs persist for more than three months and are called "chronic" PLEDs, the pathophysiology of which is still debated. Herein, we report a man with right hemispheric PLEDs which lasted for more than 14 months and mild left hemispatial neglect after he experienced status epilepticus. Although MRI was normal, positron emission tomography revealed right temporo‐parieto‐occipital hypometabolism, which coincided with the source area of PLEDs estimated by magnetoencephalography. In addition, levels of anti‐<italic>N</italic>‐methyl‐<sc>d</sc>‐aspartate (NMDA) receptor antibodies and granzyme B were found to be high in the cerebrospinal fluid. Following two courses of steroid pulse therapy, the patient's left spatial neglect improved and the PLEDs were partially resolved. These findings suggest that the chronic PLEDs present in this case were an interictal phenomenon and that their pathophysiology involved autoimmune processes.</p> </abstract>