Case Presentation of Anti-NMDA Receptor Encephalitis in a 4-Year-Old Boy

Daniel A Gbadero1, Emmanuel O Adegbite1, Jean-Baptist LePichon2

  • 1Bowen University Teaching Hospital, Ogbomoso, Oyo State 210001, Nigeria.

Insights

A Nigerian boy experienced prolonged seizures and coma, later developing involuntary movements and abnormal eye movements. This case highlights autoimmune encephalitis, specifically anti-N-methyl-D-aspartate receptor encephalitis, in a pediatric patient.

Area of Science:

  • Neuroimmunology
  • Pediatric Neurology
  • Clinical Case Study

Background:

  • Autoimmune encephalitis is an inflammatory condition affecting the brain.
  • Anti-N-methyl-D-aspartate receptor (anti-NMDAR) encephalitis is a treatable autoimmune disorder.
  • Pediatric autoimmune encephalitis can present with diverse neurological symptoms.

Observation:

  • A 4-year-old boy in Nigeria presented with prolonged seizures and coma.
  • The patient subsequently developed oro-lingual-facial dyskinesia, including tongue thrusting.
  • Additional neurological signs included dysconjugate gaze and choreoathetoid limb movements.

Findings:

  • The clinical presentation was consistent with autoimmune encephalitis.
  • Diagnostic evaluation confirmed anti-N-methyl-D-aspartate receptor (anti-NMDAR) encephalitis.
  • This case represents a pediatric presentation of anti-NMDAR encephalitis in Nigeria.

Implications:

  • Early diagnosis and treatment of anti-NMDAR encephalitis are crucial for patient outcomes.
  • This case expands the geographical understanding of anti-NMDAR encephalitis presentations.
  • Increased awareness of autoimmune encephalitis in pediatric neurology is warranted, especially in diverse populations.

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