Abstract
One of the best characterized autoimmune encephalitis is the Anti-Nmethyl- D-aspartate receptor (NMDAR) encephalitis, which may occur in the presence of cancer. First- and second-line immunotherapy and oncological investigations are suggested. We present here a case of an 18-year-old female who was our first patient suffering from Anti- NMDAR encephalitis more than 9 years ago. She was satisfactorily treated with intravenous immunoglobulins and high dose steroid therapy. After more than one year the patient had a relapse. First-line immunotherapy was repeated; however, a complete recovery was achieved only after plasmapheresis. Afterwards, she continued maintenance immunotherapy with steroids for two years and with Azathioprine for about five years associated to regular oncological assessment. In the last years our therapeutical approach of Anti-NMDARencephalitis has significantly changed. Nevertheless, established treatment guidelines are still missing and the role of long-term maintenance immunotherapy is largely unexplored. In addition, oncological revaluation might be indicated in selected patients.
Highlights
Encephalitis is an inflammatory condition of the brain with many different etiologies; several are immune mediated.[1]
We present here a case of an 18-year-old female who n was our first patient suffering from Antio N-methyl-Daspartate receptor (NMDAR) encephalitis more than 9 years ago
Anti-NMDAR encephalitis may occur in the presence or antibodies against the NMDAR in the patient’s cerebrospinal fluid (CSF) and serum demonstrating a positive result
Summary
Encephalitis is an inflammatory condition of the brain with many different etiologies; several are immune mediated.[1]. FT was the mainly responsible neurologist for the application of recent therapeutic recommendations for autoimmune encephalitis, especially of the second-line treatment.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.