| 맨아래구역 증후군과 가역적 후백질 뇌병증 증후군 양상으로 발현한 시신경척수염범주질환 |
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김동엽, 석진명, 이혜림, 조은빈, 조혜진, 김병준, 민주홍 |
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성균관대학교 의과대학 신경과학교실, 삼성서울병원 신경과 |
| A Case of Neuromyelitis Optica Spectrum Disorder Presenting as Area Postrema Syndrome with Posterior Reversible Encephalopathy Syndrome-like Feature |
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Dong Yeop Kim, Jin Myoung Seok, Hye Lim Lee, Eun Bin Cho, Hye-Jin Cho, Byoung Joon Kim, Ju-Hong Min |
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Department of Neurology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea |
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| Abstract |
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"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" |
| Key Words:
Neuromyelitis optica spectrum disorder, Area postrema syndrome, Posterior reversible encephalopathy syndrome |
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