Paraneoplastic neuromyelitis optica and ovarian teratoma: A case series

Mult Scler Relat Disord. 2019 Jun:31:97-100. doi: 10.1016/j.msard.2019.03.031. Epub 2019 Apr 1.

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.

Keywords: Autoimmune diseases; Demyelinating diseases; Neuromyelitis optica; Ovarian teratoma; Paraneoplastic syndromes.

Publication types

  • Case Reports

MeSH terms

  • Adolescent
  • Adult
  • Aquaporin 4 / metabolism
  • Female
  • Humans
  • Neuromyelitis Optica / complications*
  • Neuromyelitis Optica / diagnosis
  • Neuromyelitis Optica / metabolism
  • Neuromyelitis Optica / pathology*
  • Ovarian Neoplasms / complications*
  • Ovarian Neoplasms / diagnosis
  • Ovarian Neoplasms / metabolism
  • Ovarian Neoplasms / pathology*
  • Teratoma / complications*
  • Teratoma / diagnosis
  • Teratoma / metabolism
  • Teratoma / pathology*
  • Young Adult

Substances

  • AQP4 protein, human
  • Aquaporin 4

Supplementary concepts

  • Teratoma, Ovarian