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NMDA receptor antibody in teratoma-related opsoclonus-myoclonus syndrome.
Urriola, Nicolás X; Helou, Jacob; Maamary, Joel; Pogson, Jacob; Lee, Frederick; Parratt, Kaitlyn; Gillis, David; Fulham, Michael J; Halmágyi, G Michael.
Afiliação
  • Urriola NX; Departments of Neurology and Immunology, Royal Prince Alfred Hospital, Sydney, Australia. Electronic address: nicolas.urriola@health.nsw.gov.au.
  • Helou J; Department of Neurology, Royal Prince Alfred Hospital, Sydney, Australia.
  • Maamary J; Department of Immunology, Royal Prince Alfred Hospital, Sydney, Australia.
  • Pogson J; Department of Immunology, Royal Prince Alfred Hospital, Sydney, Australia.
  • Lee F; Department of Immunology, Royal Brisbane and Women's Hospital, Brisbane, Australia.
  • Parratt K; Department of Immunology, Royal Prince Alfred Hospital, Sydney, Australia.
  • Gillis D; Department of Medical Imaging, Royal Prince Alfred Hospital, Sydney, Australia.
  • Fulham MJ; Department of Medical Imaging, Royal Prince Alfred Hospital, Sydney, Australia.
  • Halmágyi GM; Department of Immunology, Royal Prince Alfred Hospital, Sydney, Australia.
J Clin Neurosci ; 58: 203-204, 2018 Dec.
Article em En | MEDLINE | ID: mdl-30340968
Opsoclonus-myoclonus syndrome (OMS) is a brainstem/cerebellar syndrome producing disabling multi-directional saccadic oscillations with oscillopsia, with or without somatic myoclonus and cerebellar ataxia (Wong et al., 2001; Armangué et al., 2016). OMS is presumed to have an autoimmune basis and patients with it are tested for antineuronal antibodies and have imaging to locate any tumors. Here we report a unusual case of a young woman who had NMDAR antibody (NMDAR-ab) positive, teratoma-related, isolated OMS without encephalopathy. Removal of her ovarian teratoma, and immunotherapy with steroids, intravenous immunoglobulin (IVIg), plasma exchange (PLEX), and ultimately with B-cell depletion with rituximab resulted in total recovery after 3 months. Patients with teratoma-related OMS very rarely have NMDAR-ab which suggests that it is not the NMDAR-ab per se that causes the OMS.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Ovarianas / Autoanticorpos / Teratoma / Receptores de N-Metil-D-Aspartato / Síndrome de Opsoclonia-Mioclonia Limite: Adult / Female / Humans Idioma: En Revista: J Clin Neurosci Assunto da revista: NEUROLOGIA Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Ovarianas / Autoanticorpos / Teratoma / Receptores de N-Metil-D-Aspartato / Síndrome de Opsoclonia-Mioclonia Limite: Adult / Female / Humans Idioma: En Revista: J Clin Neurosci Assunto da revista: NEUROLOGIA Ano de publicação: 2018 Tipo de documento: Article