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Anti-N-methyl-D-aspartate receptor encephalitis with an imaging-invisible ovarian teratoma: a case report.
Abdul-Rahman, Zainab M; Panegyres, Peter K; Roeck, Margareta; Hawkins, David; Bharath, Jude; Grolman, Paul; Neppe, Cliffe; Palmer, David.
Afiliación
  • Abdul-Rahman ZM; Department of Medicine, Joondalup Health Campus, Joondalup, Western Australia, Australia.
  • Panegyres PK; Academy of Neurology, Joondalup Health Campus, Joondalup, Western Australia, Australia.
  • Roeck M; Neurodegenerative Disorders Research Pty Ltd, 4 Lawrence Avenue, West Perth, Western Australia, 6005, Australia.
  • Hawkins D; Department of Medicine, Joondalup Health Campus, Joondalup, Western Australia, Australia. research@ndr.org.au.
  • Bharath J; Academy of Neurology, Joondalup Health Campus, Joondalup, Western Australia, Australia. research@ndr.org.au.
  • Grolman P; Neurodegenerative Disorders Research Pty Ltd, 4 Lawrence Avenue, West Perth, Western Australia, 6005, Australia. research@ndr.org.au.
  • Neppe C; Department of Medicine, The University of Western Australia, Perth, Western Australia, Australia. research@ndr.org.au.
  • Palmer D; Ramsay Health, Joondalup Health Campus, Joondalup, Western Australia, Australia.
J Med Case Rep ; 10(1): 296, 2016 Oct 24.
Article en En | MEDLINE | ID: mdl-27776544
ABSTRACT

BACKGROUND:

Anti-N-methyl-D-aspartate receptor encephalitis is a recently discovered disease entity of paraneoplastic limbic encephalitis. It largely affects young women and is often associated with an ovarian teratoma. It is a serious yet treatable condition if diagnosed early. Its remedy involves immunotherapy and surgical removal of the teratoma of the ovaries. This case of anti-N-methyl-D-aspartate receptor encephalitis involves an early surgical intervention with bilateral oophorectomy, despite negative imaging evidence of a teratoma. CASE PRESENTATION A 25-year-old white woman with anti-N-methyl-D-aspartate receptor encephalitis presented with behavioral changes and seizures that were confirmed to be secondary to anti-N-methyl-D-aspartate receptor encephalitis. She required an admission to our intensive care unit for ventilator support and received a number of immunological therapies. Multiple imaging investigations showed no evidence of an ovarian teratoma; she had a bilateral oophorectomy 29 days after admission. Ovarian histology confirmed the presence of a teratoma with neuronal cells. A few days after the operation she began to show signs of improvement and, apart from mild short-term memory loss, she returned to normal function.

CONCLUSIONS:

Our patient is an example of teratoma-associated anti-N-methyl-D-aspartate receptor encephalitis, in which the teratoma was identified only microscopically. Her case highlights that even with negative imaging evidence of a teratoma, ovarian pathology should still be considered and explored.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Neoplasias Ováricas / Teratoma / Encefalitis Antirreceptor N-Metil-D-Aspartato Tipo de estudio: Diagnostic_studies / Etiology_studies / Prognostic_studies Idioma: En Revista: J Med Case Rep Año: 2016 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Neoplasias Ováricas / Teratoma / Encefalitis Antirreceptor N-Metil-D-Aspartato Tipo de estudio: Diagnostic_studies / Etiology_studies / Prognostic_studies Idioma: En Revista: J Med Case Rep Año: 2016 Tipo del documento: Article