NMDA Encephalitis: Case report and literature review

NMDA Encephalitis: Case report and literature review

Authors

  • Juan Islas-Serrano Médico Interno de Pregrado, egresado de la Universidad de Sonora
  • Carlos Omar Vildaurrazaga-García Residente de tercer año de Medicina Interna en Hospital General del Estado de Sonora
  • Diana Monica Anaya-Castro Neuróloga adscrita al Hospital General del Estado de Sonora
  • Adolfo Espinoza-Larios Médico especialista en Neurocirugía, docente de la Universidad de Sonora

DOI:

https://doi.org/10.59420/remus.5.2021.22

Keywords:

Encephalitis, NMDAr, Autoimmune encephalitis

Abstract

Autoimmune encephalitis characterized by the presence of IgG antibodies to the GluR1 subunit of Nmethyl-D-Aspartate receptor (NMDAr) mainly affects women over 18 years old and is commonly associated with an ovarian teratoma. It was previously described as a paraneoplastic disease; however, it has been shown that it affects both genders and that the condition may be present without an underlying tumor. We present a case of a 20-year-old female who initially presented headaches, followed by behavioral changes. After that, she progressed to a catatonic state and central hypoventilation, requiring admission to intensive care. During her hospital stay, she presented autonomic dysfunction and dyskinesias. A serum diagnosis of anti-NMDAr encephalitis is made, starting immunosuppressive treatment with steroids, followed by rituximab. The patient had a remarkable improvement and complete recovery from the disease.

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References

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Published

2020-08-01

How to Cite

Islas-Serrano, J., Vildaurrazaga-García, C. O., Anaya-Castro, D. M., & Espinoza-Larios, A. (2020). NMDA Encephalitis: Case report and literature review: NMDA Encephalitis: Case report and literature review. REMUS - Revista Estudiantil De Medicina De La Universidad De Sonora, (5), 19–25. https://doi.org/10.59420/remus.5.2021.22

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