Reporte de un caso fatal de encefalitis autoinmunitaria asociada a teratoma ovárico

Translated title of the contribution: Report of a fatal case of autoimmune encephalitis associated with an ovarian teratoma

Santiago Rueda-Espinel, Julio Vargas-Anaya, Nathalia J. Gamarra-Ramírez

Research output: Articles / NotesScientific Articlepeer-review

Abstract

Introduction: The ovarian teratoma is the most common cell germ tumor. Some paraneoplastic syndromes have been described, including the anti-N-methyl-D-aspartate (NMDA) receptor encephalitis as part of its complications. Case report: A 22 years old female patient with no important medical history, consults due to an acute psychotic disorder and a convulsion. A meningoencephalitis was considered and broad-spectrum antibiotics and antivirals were started. Faced with deterioration, an autoimmune encephalitis is considered as well. Imaging studies revealed an ovarian teratoma and diagnosis was confirmed with antibodies against NMDA receptor in cerebrospinal fluid. Despite its resection and systemic management, the patient dies after 5 months. Discussion: The autoimmune encephalitis associated with an ovarian teratoma is rare, it's a complication that must be suspected as an exclusion diagnosis and most have a favorable prognosis, however up to a quarter of cases can be associated with irreversible damage to the hippocampal cortex and even death, mainly when late diagnosis and treatment are made. Conclusions: This case is a clinical challenge, no evidence is available since there is no standard for teratoma management. It is proposed that once a teratoma is diagnosed, an ovarian cystectomy is performed. Further studies are necessary to validate this recommendation.

Translated title of the contributionReport of a fatal case of autoimmune encephalitis associated with an ovarian teratoma
Original languageSpanish
Pages (from-to)403-409
Number of pages7
JournalRevista Chilena de Obstetricia y Ginecologia
Volume86
Issue number4
DOIs
StatePublished - 2021
Externally publishedYes

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