-
Case Report
-
J Mult Scler. 2016;7(2):55-58. Published online September 1, 2016.
- 맨아래구역 증후군과 가역적 후백질 뇌병증 증후군 양상으로 발현한 시신경척수염범주질환
-
김동엽, 석진명, 이혜림, 조은빈, 조혜진, 김병준, 민주홍
-
성균관대학교 의과대학 신경과학교실, 삼성서울병원 신경과
-
- A Case of Neuromyelitis Optica Spectrum Disorder Presenting as Area Postrema Syndrome with Posterior Reversible Encephalopathy Syndrome-like Feature
-
Dong Yeop Kim, Jin Myoung Seok, Hye Lim Lee, Eun Bin Cho, Hye-Jin Cho, Byoung Joon Kim, Ju-Hong Min
-
Department of Neurology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea
-
- Abstract
- "With the discovery of anti-aquaporin-4 antibody (AQP4-Ab), several clinical and radiological features beyond optic nerve and spinal cord were described in neuromyelitis optica (NMO). Area postremasyndrome was known to be a characteristic feature of NMO, and the association between posteriorreversible encephalopathy syndrome (PRES) and NMO was reported with the pathogenic roleof AQP4-Ab. We report a case of NMO spectrum disorder (NMOSD), initially presented with concurrentarea postrema syndrome and PRES-like feature. Journal of Multiple Sclerosis 7(2):55-58, 2016"
Keywords :Neuromyelitis optica spectrum disorder, Area postrema syndrome, Posterior reversible encephalopathy syndrome
