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Updated: Jul 26, 2026

Induction and Clinical Scoring of Chronic-Relapsing Experimental Autoimmune Encephalomyelitis
Published on: July 4, 2007
Encephalitis in Kikuchi-Fujimoto disease being immune-mediated
Shuai Chen1, Xin-Liang Liang1, Shuang He1
1Department of Neurology, Zhengzhou University People's Hospital (Henan Provincial People's Hospital), Zhengzhou, 450003, Henan, China.
Introduction:
Histiocytic necrotizing lymphadenitis, also known as Kikuchi-Fujimoto disease, is a rare benign self-limiting inflammatory disease often seen in young adults. The main clinical features are fever with cervical lymphadenopathy. Neurological complications of Kikuchi-Fujimoto disease were occasionally reported although the specific pathogenesis was not clear. The condition could be severe when encephalitis coexists.
Methods:
Here we reported a young case of Kikuchi-Fujimoto disease with subsequent severe autoimmune encephalitis.
Results:
The symmetric striatal and limbic MRI lesions combined with psycho-cognitive, epileptic symptoms supported encephalitis. Tissue-based immunofluorescence revealed widely cytoplasmic fluorescence in rat cerebellar and hippocampal neurons, which provide evidence for immune-mediated encephalitis. The clinical outcome was satisfactory after immunosuppressive therapy with MRI lesions largely disappeared.
Conclusion:
The encephalitis complication of Kikuchi disease may be autoimmune and mediated by cytotoxic T cells.
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