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Influenza-associated MOG antibody-positive longitudinally extensive transverse myelitis: a case report

2014; BioMed Central; Volume: 14; Issue: 1 Linguagem: Inglês

10.1186/s12883-014-0224-x

1471-2377

Haruka Takeshige‐Amano, Nobukazu Miyamoto, Hideki Shimura, Douglas Kazutoshi Sato, Kazuo Fujihara, Shinichi Ueno, Ryota Nakamura, Yuji Ueno, Masao Watanabe, Nobutaka Hattori, Takao Urabe,

Peripheral Neuropathies and Disorders

Myelin-oligodendrocyte glycoprotein antibody (MOG antibodies) was found in various demyelinated diseases. This is the first report of a patient with longitudinally extensive transverse myelitis with an extremely high titer of MOG antibodies after an influenza infection. This case supports the view that MOG antibodies are linked to longitudinally extensive transverse myelitis and that influenza infection might trigger the MOG antibodies.A 32-year-old healthy male developed high fever, dysesthesia and paraesthesia below the C2 area, muscle weakness of the bilateral lower extremities, and urinary retention ten days after an influenza type A infection. Magnetic resonance imaging revealed a longitudinal lesion in the spinal cord extending from C2 to the spinal conus. There were no lesions in the brain or optic nerves. Established cell-based immunoassays revealed that he was positive for MOG antibodies (titer = 65,536) and negative for anti-aquaporin 4 antibodies (AQP4 antibodies). He fully recovered after steroid pulse therapy followed by 60 mg prednisolone.This is the first report of influenza A-associated longitudinally extensive transverse myelitis with a high titer anti-MOG antibodies. Our case report supports a relationship between anti-MOG antibodies and longitudinally extensive transverse myelitis, which was triggered by influenza infection. Further studies are needed to establish the clinical significance of anti-MOG antibodies for diagnosis, treatment, and prognosis.