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

被引:37
|
作者
Amano, Haruka [1 ]
Miyamoto, Nobukazu [1 ]
Shimura, Hideki [1 ]
Sato, Douglas Kazutoshi [3 ]
Fujihara, Kazuo [3 ]
Ueno, Shinichi [1 ]
Nakamura, Ryota [1 ]
Ueno, Yuji [1 ]
Watanabe, Masao [1 ]
Hattori, Nobutaka [2 ]
Urabe, Takao [1 ]
机构
[1] Juntendo Univ, Dept Neurol, Urayasu Hosp, Chiba 2790021, Japan
[2] Juntendo Univ, Sch Med, Dept Neurol, Tokyo 113, Japan
[3] Tohoku Univ, Grad Sch Med, Dept Neurol, Sendai, Miyagi 980, Japan
来源
BMC NEUROLOGY | 2014年 / 14卷
关键词
Myelin-oligodendrocyte glycoprotein antibody; Longitudinal extensive transverse myelitis; Neuromyelitis optica; Aquaporin-4; antibody; OLIGODENDROCYTE GLYCOPROTEIN ANTIBODIES; NEUROMYELITIS-OPTICA; NEUROLOGIC COMPLICATIONS; SPECTRUM DISORDERS; PEDIATRIC-PATIENTS; NEURITIS; MICE; ENCEPHALOMYELITIS; AQUAPORIN-4; COOPERATE;
D O I
10.1186/s12883-014-0224-x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: 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. Case presentation: 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. Conclusion: 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.
引用
收藏
页数:4
相关论文
共 50 条
  • [21] Myelin oligodendrocyte glycoprotein (MOG) antibody-associated longitudinally extensive transverse myelitis (LETM) and primary Sjogren syndrome: a rare association
    Sahoo, Debananda
    Dash, Anil
    Dey, Anupam
    Devi, Sujata
    BMJ CASE REPORTS, 2022, 15 (12)
  • [22] A case of MOG antibody disoorder with pontine involvement mimicking CLIPPERS and extensive transverse myelitis
    Keroles, Mark
    Stocksdale, Brian
    Ng, Jessica
    Ahadi, Sahar
    Dunn, Jeffrey
    NEUROLOGY, 2022, 98 (18)
  • [23] MRI Features of Aquaporin-4 Antibody-Positive Longitudinally Extensive Transverse Myelitis: Insights into the Diagnosis of Neuromyelitis Optica Spectrum Disorders
    Chee, C. G.
    Park, K. S.
    Lee, J. W.
    Ahn, H. W.
    Lee, E.
    Kang, Y.
    Kang, H. S.
    AMERICAN JOURNAL OF NEURORADIOLOGY, 2018, 39 (04) : 782 - 787
  • [25] A Rare Case of Longitudinally Extensive Transverse Myelitis Following Febrile Illness: A Case Report
    Wettasinghe, Indika
    Puthra, Shiran
    Sugathapala, Hemal A.
    Mendis, Suresh
    CUREUS JOURNAL OF MEDICAL SCIENCE, 2024, 16 (03)
  • [26] Neurosarcoidosis Presenting as Longitudinally Extensive Transverse Myelitis and Orbital Mass: A Case Report
    Cassimatis, Nicholas
    Hong, Ellen
    Trippiedi, Andrew
    Lauer, Simeon A.
    CUREUS JOURNAL OF MEDICAL SCIENCE, 2023, 15 (04)
  • [28] Neurobrucellosis presenting as longitudinally extensive transverse myelitis: A case report and review of the literature
    Yamout, B., I
    Massouh, J.
    Hushaymi, I
    Zeineddine, M.
    Saab, G.
    MULTIPLE SCLEROSIS AND RELATED DISORDERS, 2020, 40
  • [29] Isolated recurrent non longitudinally extensive myelitis in two mog positive patients
    Valero Lopez, G.
    Carreon Guarnizo, E.
    Moreno Arjona, M. D. L. P.
    Hernandez Clares, R.
    Morales De la Prida, M.
    Canovas Iniesta, M.
    Iniesta Martinez, F.
    Morales Ortiz, A.
    Meca-Lallana, J.
    MULTIPLE SCLEROSIS JOURNAL, 2020, 26 (3_SUPPL) : 463 - 464
  • [30] MOG-IgG longitudinally extensive transverse myelitis in a patient with systemic lupus erythematosus
    Bilodeau, P. A.
    Kumar, V.
    Rodriguez, A.
    Li, C.
    Sanchez-Alvarez, C.
    Thanarajasingam, U.
    Zalewski, N.
    Flanagan, E.
    MULTIPLE SCLEROSIS JOURNAL, 2019, 25 : 808 - 809