Paraneoplastic anti-NMDA receptor encephalitis in 1830?

Neurol Neuroimmunol Neuroinflamm. 2020 Sep 25;7(6):e887. doi: 10.1212/NXI.0000000000000887. Print 2020 Nov.

Abstract

Objective: Our aim was to identify patients with probable anti-NMDA receptor encephalitis among historical medical cases.

Method: A case report published in leading Hungarian-, German- and Italian-language medical journals in the early 1840s was revisited.

Results: In 1830, an 18-year-old, healthy woman suffered epileptic seizures, followed by a 6-day-long state characterized by catalepsy, unresponsiveness, motionless, and light breathing. Her symptoms regularly returned in the following 1.5 years. Meanwhile, a progressively growing huge abdominal tumor appeared. One day, she suddenly started vomiting a large amount of foul-smelling pus mixed with blood, accompanied by bone fragments. Pus mixed blood with some membranous substance was also evacuated through the anus and vagina. After this event, she completely recovered; 1.5 years later, she married and later gave birth to 3 healthy children. The patient remained healthy during the 11-year follow-up.

Conclusions: We suggest that in the description of a paraneoplastic case, an anti-NMDA receptor encephalitis can be dated back as far as to the 19th century, with an especially rare type of resolution: the disappearance of the symptoms after the spontaneous elimination of an ovarian teratoma.

Publication types

  • Historical Article
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Anti-N-Methyl-D-Aspartate Receptor Encephalitis / diagnosis
  • Anti-N-Methyl-D-Aspartate Receptor Encephalitis / etiology
  • Anti-N-Methyl-D-Aspartate Receptor Encephalitis / history*
  • Anti-N-Methyl-D-Aspartate Receptor Encephalitis / physiopathology
  • Female
  • History, 19th Century
  • Humans
  • Ovarian Neoplasms / complications
  • Teratoma / complications
  • Young Adult