AI Article Synopsis

  • Anti-methyl-D-aspartate receptor encephalitis can be mistaken for Hashimoto's encephalopathy due to similar symptoms like delirium, seizures, and behavioral changes.
  • A young female with subclinical hypothyroidism was misdiagnosed, experiencing elevated thyroid antibodies, before the correct diagnosis was made through testing her cerebrospinal fluid.
  • After receiving treatment with intravenous immunoglobulin and other medications, she showed significant recovery with minor lasting effects after three weeks.

Article Abstract

Anti--methyl-D-aspartate receptor encephalitis is a life-threatening medical emergency that can be clinically misperceived as Hashimoto's encephalopathy. We present a case of anti--methyl-D-aspartate receptor encephalitis in an otherwise healthy young female with subclinical hypothyroidism without an associated ovarian teratoma. She was first misdiagnosed as Hashimoto's encephalopathy due to delirium and behavioral changes, seizures, psychosis, and increased amount of thyroid peroxidase and thyroglobulin antibodies in serum. Final diagnosis was established by third week following presentation with the detection of anti--methyl-D-aspartate receptor antibodies in her cerebrospinal fluid. After treatment with intravenous immunoglobulin, methylprednisolone, and amisulpride, she recovered significantly with minimal sequelae at 3-week follow-up.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7443984PMC
http://dx.doi.org/10.1177/2050313X20949780DOI Listing

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