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Anti-CASPR2 encephalitis in a liver posttransplant patient receiving immune-suppression and lenvatinib: a case report and literature review

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Abstract

It has been assumed that patients with strict immunosuppressive treatment after solid organ transplantation have only marginal risk in developing autoimmune encephalitis. We reported a woman in her late 40 s who presented with generalized convulsions and loss of consciousness. After detailed history review, neuropsychological tests, metagenomic next-generation sequencing of serum and cerebrospinal fluid (CSF), magnetic resonance imaging (MRI) brain, and electroencephalogram, she was diagnosed as anti-CASPR2 encephalitis based on the positive anti-CASPR2 auto-antibody in serum and CSF. The patient underwent liver transplantation and has taken lenvatinib for 2 months, in addition to tacrolimus, mycophenotale mofetil, and entecavir administered for half a year. This case was the first report of anti-CASPR2 encephalitis in post–organ transplantation patients. Together with the reports of other encephalitis cases in organ transplantation, it warns the possibility of developing immune-oriented encephalitis in patients undergoing immunosuppression, especially in combination with other treatments of immunomodulatory activity.

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Data availability

The data that support the findings of this study are available from the corresponding author upon reasonable request.

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Funding

This study was supported by the Hospital Management Fund of Sichuan Provincial People’s Hospital (2021481).

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NWY and JL designed the study. BLD and SSH collected data. DZW, BHL, FQG, and JL drafted the manuscript. All authors critically revised, read, and approved the final manuscript.

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Correspondence to Neng-Wei Yu or Jie Liu.

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The participant as well as her family has consented to the publication of the case report to the journal.

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Wang, DZ., Li, BH., Deng, BL. et al. Anti-CASPR2 encephalitis in a liver posttransplant patient receiving immune-suppression and lenvatinib: a case report and literature review. Neurol Sci 44, 1069–1072 (2023). https://doi.org/10.1007/s10072-022-06560-4

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  • DOI: https://doi.org/10.1007/s10072-022-06560-4

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