Lymphomatosis cerebri with coexistent anti-N-methyl-D-aspartate receptor antibody: A case report.
Natthapon RattanathamsakulTatchaporn OngphichetmethaPattharasaya WeerachotisakulNanthaya TisavipatPornsuk CheunsuchonJiraporn JitprapaikulsanPublished in: Neuropathology : official journal of the Japanese Society of Neuropathology (2023)
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.
Keyphrases
- white matter
- magnetic resonance imaging
- cerebrospinal fluid
- multiple sclerosis
- simultaneous determination
- immune response
- spinal cord injury
- computed tomography
- case report
- mass spectrometry
- liquid chromatography
- diffuse large b cell lymphoma
- high resolution
- cerebral palsy
- small cell lung cancer
- randomized controlled trial
- low dose
- clinical trial
- early onset
- subarachnoid hemorrhage
- newly diagnosed
- botulinum toxin