Gahr Maximilian, Lauda Florian, Wigand Moritz E, Connemann Bernhard J, Rosenbohm Angela, Tumani Hayrettin, Reindl Markus, Uzelac Zeljko, Lewerenz Jan
Department of Psychiatry and Psychotherapy III, University of Ulm, Leimgrubenweg 12-14, 89075 Ulm, Germany.
Department of Neurology, University of Ulm, Oberer Eselsberg 45, 89081 Ulm, Germany.
BMJ Case Rep. 2015 Apr 26;2015:bcr2014209075. doi: 10.1136/bcr-2014-209075.
Several findings suggest that there may be an overlap of anti-N-methyl-d-aspartate receptor (NMDAR) antibody encephalitis with neuromyelitis optica spectrum disorders or acute demyelinating encephalomyelitis (ADEM)-like demyelination. We present a case of a patient with anti-NMDAR antibody encephalitis, who on MRI featured a single prominent T2-hyperintensive white matter lesion in the periventricular region, adjacent to the anterior horn of the left lateral ventricle. In view of the lesion location and the cerebrospinal fluid (CSF) findings (incomplete MRZ (measles, rubella and varicella zoster) reaction, lymphocytic pleocytosis, intrathecal IgG and IgM synthesis; absence of aquaporin-4 (AQP4) and myelin oligodendrocyte glycoprotein (MOG) antibodies), the presence of a multiple sclerosis-like immune response was discussed. This case appears to add evidence to the hypothesis of an overlap between anti-NMDAR antibody encephalitis and other inflammatory central nervous system diseases.
多项研究结果表明,抗N-甲基-D-天冬氨酸受体(NMDAR)抗体脑炎可能与视神经脊髓炎谱系障碍或急性脱髓鞘性脑脊髓炎(ADEM)样脱髓鞘存在重叠。我们报告一例抗NMDAR抗体脑炎患者,其MRI表现为脑室周围区域单个明显的T2高信号白质病变,毗邻左侧脑室前角。鉴于病变位置及脑脊液(CSF)检查结果(MRZ(麻疹、风疹和水痘带状疱疹)反应不完全、淋巴细胞增多、鞘内IgG和IgM合成;水通道蛋白4(AQP4)和髓鞘少突胶质细胞糖蛋白(MOG)抗体阴性),讨论了是否存在类似多发性硬化的免疫反应。该病例似乎为抗NMDAR抗体脑炎与其他炎症性中枢神经系统疾病存在重叠这一假说增添了证据。