Exploring the coexistence of anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis and demyelinating disorders in a pediatric case
Year: 2025
Type: article
Study design: Case Report
Abstract: Anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis is an immune-mediated disorder characterized by a complex neuropsychiatric syndrome and the presence of cerebrospinal fluid antibodies targeting the GluN1 subunit of the NMDAR. While well-documented, its association with demyelinating disorders—such as neuromyelitis optica, myelitis, and acute disseminated encephalomyelitis—remains rare, particularly in pediatric cases. Here, we present an unusual case of a 7-year-old female who initially exhibited area postrema syndrome, followed by acute brainstem syndrome and encephalopathy. Over two subsequent relapses within 2 years, she developed longitudinally extensive transverse myelitis, seizures, and diencephalic syndrome, alongside mild contrast-enhancing lesions in both infratentorial and supratentorial regions. Despite repeated testing, both antibodies to myelin-oligodendrocyte glycoprotein and aquaporin-4 remained negative. Subsequently, a comprehensive antibody testing protocol, including indirect immunohistochemistry on rat brain tissue and an extensive panel of both fixed and live cell-based assays was requested, confirming the presence of anti-NMDAR antibodies, along with superimposed reactivity to cerebellar granular cells. This report explores the diagnostic and therapeutic complexities of coexisting anti-NMDAR encephalitis and demyelinating disorders. The rarity of this overlap and its distinct clinical features underscore the need for further research into the immunological mechanisms underlying these conditions. • Diagnostic delay and misrecognition are common in overlapping anti-NMDAR encephalitis and demyelinating disorders, especially when initial symptoms resemble conditions such as ADEM or NMOSD. • Anti-NMDAR encephalitis should be considered in pediatric demyelinating cases presenting with prominent psychiatric or behavioral symptoms. • Long-term monitoring is essential in overlapping autoimmune syndromes due to the potential for recurrence driven by distinct immune pathways.
Source: Medical Reports
Authors: Louise Scridelli Tavares, Felipe Augusto Folha Santos, Marianna Pinheiro Moraes de Moraes, Ricardo Pinho Silva, Marcelo de Melo Aragão, Enedina Maria Lobato de Oliveira
Institution: Universidade Federal de São Paulo
Language: English
Subfield: Neurology
Field: Medicine
Domain: Health Sciences
Open Access status: hybrid
Estimated APC paid: $1,900
OpenAlex ID: W4414421383