Paraneoplastic anti-NMDA receptor encephalitis in 1830?

被引:3
|
作者
Tenyi, Dalma [1 ]
Szucs, Anna [2 ]
Kovacs, Norbert [1 ,3 ]
Illes, Zsolt [4 ,5 ]
Janszky, Jozsef [1 ,3 ]
机构
[1] Univ Pecs, Med Sch, Dept Neurol, Pecs, Hungary
[2] Natl Inst Clin Neurosci, Budapest, Hungary
[3] MTA PTE Clin Neurosci MRI Res Grp, Budapest, Hungary
[4] Odense Univ Hosp, Dept Neurol, Odense, Denmark
[5] Univ Southern Denmark, Dept Clin Res, Odense, Denmark
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D O I
10.1212/NXI.0000000000000887
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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.
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