| Literature DB >> 28101360 |
Elzbieta Rypulak1, Michal Borys1, Pawel Piwowarczyk1, Magdalena Fijalkowska1, Beata Potrec1, Justyna Sysiak1, Janusz Spustek2, Alicja Bartkowska-Sniatkowska3, Jan Kotarski4, Waldemar A Turski5, Konrad Rejdak6, Miroslaw Czuczwar1.
Abstract
Anti-N-methyl-d-aspartate-receptor (NMDAR) encephalitis is an uncommon autoimmune disorder with a wide spectrum of neuropsychiatric symptoms. There is a great requirement to emphasize the importance of a multidisciplinary team approach in the process of diagnosis and treatment of the potentially fatal condition, including psychiatrists, neurologists, gynaecologists and intensivists. Physicians must be aware that psychiatric and neurological disorders, which are typical features for NMDAR encephalitis in young women with ovarian tumours, may progress into status epilepticus and respiratory insufficiency. This disease can only be successfully treated with prompt surgical intervention and an early implementation of a wide array of immunosuppressive therapies. Optimal timing of initiation of therapeutic plasma exchange, as well as duration of treatment necessary to achieve desirable outcomes in patients with NMDAR remains unknown. The present case report aims to raise awareness about the importance of early implementation of this potentially life-saving therapy and continuing the treatment courses until full subsidence of symptoms.Entities:
Keywords: EEG abnormalities; anti-NMDA receptor antibodies; autoimmune encephalitis; status epilepticus; therapeutic plasma exchange
Year: 2016 PMID: 28101360 PMCID: PMC5228193 DOI: 10.3892/mco.2016.1054
Source DB: PubMed Journal: Mol Clin Oncol ISSN: 2049-9450