Artigo Acesso aberto Revisado por pares

Neuromyelitis Optica in a Young Child With Positive Serum Autoantibody

2008; Elsevier BV; Volume: 39; Issue: 3 Linguagem: Inglês

10.1016/j.pediatrneurol.2008.05.016

ISSN

1873-5150

Autores

Ingrid P. Loma, Miya R. Asato, Robyn A. Filipink, Gülay Alper,

Tópico(s)

Systemic Lupus Erythematosus Research

Resumo

Relapsing neuromyelitis optica is rare in children. The identification of a highly specific serum autoantibody marker (neuromyelitis optica-immunoglobulin G) differentiates neuromyelitis optica from other demyelinating disorders, particularly in clinically challenging cases. We present a child with multiple episodes of transverse myelitis and optic neuritis with positive neuromyelitis optica-immunoglobulin G titers, consistent with a diagnosis of relapsing neuromyelitis optica. Serial titers of neuromyelitis optica-immunoglobulin G normalized during remission. Relapsing neuromyelitis optica is rare in children. The identification of a highly specific serum autoantibody marker (neuromyelitis optica-immunoglobulin G) differentiates neuromyelitis optica from other demyelinating disorders, particularly in clinically challenging cases. We present a child with multiple episodes of transverse myelitis and optic neuritis with positive neuromyelitis optica-immunoglobulin G titers, consistent with a diagnosis of relapsing neuromyelitis optica. Serial titers of neuromyelitis optica-immunoglobulin G normalized during remission.

Referência(s)