视神经脊髓炎
横贯性脊髓炎
多发性硬化
医学
视神经炎
光谱紊乱
脊髓炎
脱髓鞘病
水通道蛋白4
脱髓鞘病
病理
疾病
皮肤病科
脊髓
免疫学
精神科
作者
Lucas Cornelis van Rooij,Mike P. Wattjes,Brigit A. de Jong,Bob W. van Oosten
标识
DOI:10.1016/j.msard.2017.06.009
摘要
Background MS is a demyelinating CNS disease and has distinct clinical and radiological features. Neuromyelitis optica spectrum disorder (NMOSD) is an antibody related auto-immune disease known for invalidating episodes of myelitis and optic neuritis. Objective Reporting the case of a 29-year old woman with a disease course typical for relapsing remitting MS with consistent radiological and spinal fluid findings, who developed longitudinally extensive transverse myelitis (LETM) with positive aquaporin 4 antibodies, fulfilling the diagnostic criteria for NMOSD. Methods Case report. Results LETM is not consistent with MS. Consider NMOSD even in patients with typical MS and check for aquaporin-4 antibodies, with important treatment consequences.
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