Lymphomatosis cerebri with coexistent anti-N-methyl-D-aspartate receptor antibody: A case report

被引:1
作者
Rattanathamsakul, Natthapon [1 ,2 ]
Ongphichetmetha, Tatchaporn [2 ]
Weerachotisakul, Pattharasaya [3 ]
Tisavipat, Nanthaya [2 ]
Cheunsuchon, Pornsuk [3 ,4 ]
Jitprapaikulsan, Jiraporn [1 ,2 ]
机构
[1] Mahidol Univ, Fac Med, Dept Med, Div Neurol,Siriraj Hosp, Bangkok, Thailand
[2] Mahidol Univ, Fac Med, Siriraj Neuroimmunol Ctr, Dept Med,Siriraj Hosp, Bangkok, Thailand
[3] Mahidol Univ, Fac Med, Siriraj Hosp, Bangkok, Thailand
[4] Mahidol Univ, Fac Med, Dept Pathol, Siriraj Hosp, Bangkok, Thailand
关键词
acute disseminated encephalomyelitis; anti-N-methyl-D-aspartate receptor; autoimmune encephalitis; lymphoma; lymphomatosis cerebri;
D O I
10.1111/neup.12899
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Diagnosis of lymphomatosis cerebri (LC) is usually delayed because of its rarity and the need for pathological confirmation. The association of LC with humoral immunity has scarcely been reported. Herein, we present a woman with a 2-week history of dizziness and gait ataxia, followed by diplopia, altered mental status, and spasticity of all limbs. Magnetic resonance imaging (MRI) of the brain showed multifocal lesions involving bilateral subcortical white matter, deep gray structures, and brainstem. Oligoclonal bands and anti-N-methyl-D-aspartate receptor (NMDAR) antibodies were present in cerebrospinal fluid (CSF) twice. She was initially treated with methylprednisolone but still worsening. A stereotactic brain biopsy confirmed the diagnosis of LC. This is a report on the distinctive coexistence of the rare CNS lymphoma variant and the anti-NMDAR antibody.
引用
收藏
页码:403 / 407
页数:5
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