High-dose intravenous immunoglobulin for the treatment of MUSK antibody-positive seronegative myasthenia gravis

被引:18
|
作者
Takahashi, Hirokatsu [1 ]
Kawaguchi, Naoki [1 ]
Nemoto, Yuko [1 ]
Hattori, Takamichi [1 ]
机构
[1] Chiba Univ, Grad Sch Med, Dept Neurol, Chuo Ku, Chiba 2608670, Japan
关键词
myasthenia gravis (MG); seronegative mg; high-dose intravenous gammaglobulin (IVIg); anti-muscle specific tyrosine kinase (MuSK)-antibody;
D O I
10.1016/j.jns.2006.05.065
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
We treated two patients with anti-muscle specific tyrosine kinase (MuSK)-antibody positive seronegative myasthenia gravis (MG) with high-dose intravenous gammaglobulin (IVIg) and evaluated their clinical courses. Both patients were Japanese women, MUSK-positive seronegative MG, and were unresponsive to conventional treatments, including thymectomy, steroids, and tacrolimus. The patients required frequent hospitalization for plasmapheresis. In case 1, a 45-year-old woman, it was difficult to obtain blood access for plasmapheresis. High-dose IVIg, 400 mg/kg per day for 5 days, was administered in cases 1 and 2. In both cases, clinical improvement was observed 3 days after the start of IVIg therapy and lasted for 2 to 3 months. We propose that IVIg therapy is an effective treatment for MUSK-positive seronegative MG, when conventional treatments have failed. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:239 / 241
页数:3
相关论文
共 50 条
  • [31] Successful long-term treatment of MuSK antibody-positive myasthenia gravis with rituximab, a follow up
    Jordan, B.
    Eger, K.
    Deschauer, M.
    Zierz, S.
    NEUROMUSCULAR DISORDERS, 2007, 17 (9-10) : 819 - 819
  • [32] Oral salbutamol for symptomatic treatment in MuSK antibody-positive myasthenia gravis: a single-centre experience
    Baheerathan, A.
    Dorsey, R.
    Viegas, S.
    ACTA NEUROLOGICA BELGICA, 2024, 124 (05) : 1737 - 1738
  • [33] High-dose cyclophosphamide in refractory myasthenia gravis with MuSK antibodies
    Lin, PT
    Martin, BA
    Weinacker, AB
    So, YT
    MUSCLE & NERVE, 2006, 33 (03) : 433 - 435
  • [34] Familial MuSK antibody positive myasthenia gravis
    Ekmekci, O.
    Yuceyar, A.
    Karasoy, H.
    NEUROMUSCULAR DISORDERS, 2015, 25 : S208 - S208
  • [35] Anti-MuSK Antibody-positive Myasthenia Gravis Mimicking Amyotrophic Lateral Sclerosis
    Furuta, Natsumi
    Ishizawa, Kunihiko
    Shibata, Makoto
    Tsukagoshi, Setsuki
    Nagamine, Shun
    Makioka, Kouki
    Fujita, Yukio
    Ikeda, Masaki
    Yoshimura, Shunsuke
    Motomura, Masakatsu
    Okamoto, Koichi
    Ikeda, Yoshio
    INTERNAL MEDICINE, 2015, 54 (19) : 2497 - 2501
  • [36] ON THE MECHANISM OF HIGH-DOSE INTRAVENOUS IMMUNOGLOBULIN (IVIG) ACTION IN MYASTHENIA-GRAVIS (MG)
    MOREL, E
    LIBLAU, R
    GAJDOS, P
    JOURNAL OF NEUROIMMUNOLOGY, 1987, 16 (01) : 128 - 128
  • [37] MuSK antibody positive myasthenia gravis: Response to treatment in 31 patients
    Sanders, Donald
    Massey, Janice
    Juel, Vern
    NEUROLOGY, 2007, 68 (12) : A299 - A299
  • [38] HIGH-DOSE INTRAVENOUS METHYLPREDNISOLONE IN MYASTHENIA-GRAVIS
    ARSURA, E
    BRUNNER, NG
    NAMBA, T
    GROB, D
    ARCHIVES OF NEUROLOGY, 1985, 42 (12) : 1149 - 1153
  • [39] Musk antibody positive myasthenia gravis with enlarged thymus
    Dhand, UK
    Burger, RC
    MUSCLE & NERVE, 2005, 32 (03) : 416 - 416
  • [40] The prevalence of MuSK antibody positive myasthenia gravis worldwide
    Vincent, A.
    Lang, B.
    JOURNAL OF NEUROIMMUNOLOGY, 2006, 178 : 233 - 233