| Literature DB >> 30954932 |
Raphaël Bernard-Valnet1, Alvaro Cobo-Calvo2, Aurore Siegfried3, Raluca Marasescu4, Mickael Bonnan4, Guillaume Ballan5, Emmanuel Ellie5, Jan Bauer6, Emmanuelle Uro-Coste3, Romain Marignier2, David Brassat7.
Abstract
Neuromyelitis optica spectrum disorder (NMOSD) is a rare inflammatory disease of the central nervous system, characterized by the presence of auto-antibodies directed against aquaporin-4 (AQP4) expressed on astrocyte end-feet. Despite NMOSD does not primarily belong to the spectrum of paraneoplastic neurological syndromes, rare cases of association with neoplasia have been outlined. Here, we report the association of NMOSD with ovarian teratoma in 3 cases. Pathological analysis of teratomas revealed glial component strongly expressing AQP4 and closely localized to immune infiltrates. Our series highlight the rare association of teratoma with NMOSD and the possible paraneoplastic mechanism.Entities:
Keywords: Autoimmune diseases; Demyelinating diseases; Neuromyelitis optica; Ovarian teratoma; Paraneoplastic syndromes
Year: 2019 PMID: 30954932 DOI: 10.1016/j.msard.2019.03.031
Source DB: PubMed Journal: Mult Scler Relat Disord ISSN: 2211-0348 Impact factor: 4.339