MDS Abstracts

Abstracts from the International Congress of Parkinson’s and Movement Disorders.

MENU 
  • Home
  • Meetings Archive
    • 2024 International Congress
    • 2023 International Congress
    • 2022 International Congress
    • MDS Virtual Congress 2021
    • MDS Virtual Congress 2020
    • 2019 International Congress
    • 2018 International Congress
    • 2017 International Congress
    • 2016 International Congress
  • Keyword Index
  • Resources
  • Advanced Search

An extraordinary cause of psychosis: Anti-NMDA receptor encephalitis

H. Batur Caglayan, F. Sahin, T. Altıparmak, E. Turksoy, S. Candansayar, A. Bora Tokcaer (Ankara, Turkey)

Meeting: 2018 International Congress

Abstract Number: 841

Keywords: Catatonia, NMDA, Psychosis

Session Information

Date: Sunday, October 7, 2018

Session Title: Other

Session Time: 1:45pm-3:15pm

Location: Hall 3FG

Objective: Anti-N-methyl-D-aspartate (anti-NMDA) receptor encephalitis is an autoimmune encephalitis affecting predominantly young females.

Background: It is characterized with neuropsychiatric symptoms, including personality changes, psychosis, autonomic dysfunction, seizures and movement disorders.

Methods: We describe a young woman with anti-NMDA receptor encephalitis who presents with psychotic symptoms and catatonia.

Results: A 19 year-old woman admitted to our outpatient clinic with a history of headache, papilledema for two years, depression for one year and delusions for 2 weeks. Her past medical history revealed ulcerative colitis (UC) and idiopathic intracranial hypertension(IIH). She was on mesalazine and azathiopirine therapy for UC. Acetazolamide and repeated lumbar punction (13 times) had been recommended for IIH in another clinic. Her neurological examination was normal except for apathy, catatonic posture. Her psychiatric examination revealed apathy, insomnia, food refusal and non-systematic paranoid delusions. Brain MRI showed dural thickening and meningeal contrast enhancement especially on frontoparietal cortex. CSF findings identified lymphocytic pleocytosis and CSF protein levels were 187,8 mg/dl. High titers of Anti-NMDA receptor antibodies were present in CSF with a dilution of 1/1000. The proportion of CD19+ B-cells was %6.6. Abdominal ultrasonography and MRI was normal. The patient was diagnosed with tumor negative anti-NMDA receptor encephalitis. She was treated with olanzapine for psychiatric manifestations, intravenous immunoglobulin (IVIG), 0.4 g/kg/d for 5 days and methylprednisolone IV 500 mg/d for 10 days as first line therapy. Because of partial neurological improvement, rituximab 100 mg/ week was administered as the second line therapy.

Conclusions: Anti-NMDAR encephalitis is a treatment responsive encephalitis leading to death and devastating neurological sequelae. The diagnosis is based on clinical suspicion and the detection of antibodies against NMDA receptors in CSF. Early recognition and treatment of anti-NMDAR encephalitis is essential for recovery of neuropsychiatric manifestations of the disease.

To cite this abstract in AMA style:

H. Batur Caglayan, F. Sahin, T. Altıparmak, E. Turksoy, S. Candansayar, A. Bora Tokcaer. An extraordinary cause of psychosis: Anti-NMDA receptor encephalitis [abstract]. Mov Disord. 2018; 33 (suppl 2). https://www.mdsabstracts.org/abstract/an-extraordinary-cause-of-psychosis-anti-nmda-receptor-encephalitis/. Accessed June 14, 2025.
  • Tweet
  • Click to email a link to a friend (Opens in new window) Email
  • Click to print (Opens in new window) Print

« Back to 2018 International Congress

MDS Abstracts - https://www.mdsabstracts.org/abstract/an-extraordinary-cause-of-psychosis-anti-nmda-receptor-encephalitis/

Most Viewed Abstracts

  • This Week
  • This Month
  • All Time
  • Humor processing is affected by Parkinson’s disease and levodopa
      • Help & Support
      • About Us
      • Cookies & Privacy
      • Wiley Job Network
      • Terms & Conditions
      • Advertisers & Agents
      Copyright © 2025 International Parkinson and Movement Disorder Society. All Rights Reserved.
      Wiley