| Literature DB >> 28638692 |
Hiroshi Oiwa1,2, Toru Yamabe2, Masanori Kawashima3, Yuta Maetani4, Dai Agari4, Takemori Yamawaki4, Eiji Sugiyama5.
Abstract
Lupus myelitis (LM) is a rare but serious complication of systemic lupus erythematosus (SLE). In 2009, Birnbaum et al. suggested that LM could be classified into two subtypes, namely gray and white matter myelitis, based on neurological examination findings. Here we describe three cases of this disorder, one with signs of white matter dysfunction and two with signs of gray matter dysfunction. We discuss the potential role of autoantibodies in the development of LM.Entities:
Keywords: Lupus myelitis; anti-cardiolipin antibody; anti-cardiolipin beta-2 glicoprotein-1 antibody; lupus anti-coagulant; systemic lupus erythematosus; transverse myelitis
Year: 2017 PMID: 28638692 PMCID: PMC5473454 DOI: 10.5152/eurjrheum.2017.160099
Source DB: PubMed Journal: Eur J Rheumatol ISSN: 2147-9720