`The Association of methylprednisolone dosing to cessation of myotonia in a patient with myotonic dystrophy type 1

被引:0
|
作者
Horakova, Magda [1 ,2 ]
Horak, Tomas [1 ,2 ]
Bednarik, Josef [1 ,2 ]
Vohanka, Stanislav [1 ,2 ]
机构
[1] Univ Hosp Brno, ERN EURO NMD Ctr, Dept Neurol, Brno, Czech Republic
[2] Masaryk Univ, Fac Med, Brno, Czech Republic
关键词
Myotonia; Myotonic dystrophy; Methylprednisolone; Corticosteroids; Muscle relaxation; Therapy; CHANNEL;
D O I
10.1016/j.nmd.2020.03.004
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
We report the case of a patient suffering from duplicity of myotonic dystrophy type 1 and ulcerative colitis whose treatment for ulcerative colitis included repeated administrations of descending doses of methylprednisolone and in whom we found an association between methylprednisolone dosing and cessation of myotonia. Myotonia severity was expressed as relaxation time after voluntary contraction and as a patient-reported outcome using the Czech version of the Myotonia Behavior Scale. The patient was being treated for a flare of ulcerative colitis, starting with 32 mg of methylprednisolone and reducing the dose by 4 mg a week. The symptoms of myotonia began to wear off three weeks after starting methylprednisolone and had totally disappeared by four weeks after starting methylprednisolone. The first symptoms of myotonia returned about a month after the last dose of methylprednisolone and reached a peak of severity more than two months after the final dose. (C) 2020 Elsevier B.V. All rights reserved.
引用
收藏
页码:427 / 430
页数:4
相关论文
共 50 条
  • [41] Long-term effects of mexiletine on myotonia and on the cardiac conduction system of patients with myotonic dystrophy type 1
    Meola, G
    Sansone, V
    De Ambroggi, L
    Gandossini, S
    Cotelli, M
    JOURNAL OF NEUROLOGY, 2005, 252 : 25 - 25
  • [42] Generalized epilepsy in a patient with myotonic dystrophy type 2
    Cagnetti, C.
    Buratti, L.
    Foschi, N.
    Balestrini, S.
    Provinciali, L.
    NEUROLOGICAL SCIENCES, 2014, 35 (03) : 489 - 490
  • [43] Atypical diabetes in a patient with myotonic dystrophy type 2
    Aguirre, Roxana L.
    Lteif, Aida
    HORMONE RESEARCH, 2009, 72 : 177 - 178
  • [44] Multiple Follicular Hybrid Tumors Presenting in Association With Myotonic Dystrophy Type 1
    Wang, Robin H.
    Krouse, Adam
    Eilers, David B.
    Dahiya, Madhu
    AMERICAN JOURNAL OF DERMATOPATHOLOGY, 2024, 46 (11) : 771 - 773
  • [45] Myotonic dystrophy: clinical and molecular parallels between myotonic dystrophy type 1 and type 2.
    Ranum L.P.
    Day J.W.
    Current Neurology and Neuroscience Reports, 2002, 2 (5) : 465 - 470
  • [46] Generalized epilepsy in a patient with myotonic dystrophy type 2
    C. Cagnetti
    L. Buratti
    N. Foschi
    S. Balestrini
    L. Provinciali
    Neurological Sciences, 2014, 35 : 489 - 490
  • [47] Undiagnosed myotonic dystrophy type 1 in a patient with synchronous thymoma and thyroid cancer
    Gomez Hernandez, M. Teresa
    Martin Posadas, M. Teresa
    Gonzalez Sanchez, M. del Carmen
    ARCHIVOS DE BRONCONEUMOLOGIA, 2016, 52 (07): : 393 - 394
  • [48] Sporadic Myotonic Dystrophy Type 2 in a Japanese Patient
    Miyashita, Koichi
    Ii, Yuichiro
    Matsuyama, Hirofumi
    Niwa, Atsushi
    Kawana, Yosuke
    Shibata, Soshi
    Minami, Narihiro
    Nishino, Ichizo
    Tomimoto, Hidekazu
    INTERNAL MEDICINE, 2023, 62 (20) : 3027 - 3031
  • [49] A rare bimodal distribution of expanded alleles in a patient with myotonic dystrophy type 1
    Stopps, K
    King, W
    Taylor, R
    Norbury, G
    Flinter, F
    JOURNAL OF MEDICAL GENETICS, 2003, 40 : S71 - S71
  • [50] Atrial flutter in myotonic dystrophy type 1: patient characteristics and clinical outcome
    Wahbi, K.
    Sebag, F. A.
    Lellouche, N.
    Lazarus, A.
    Becane, H. -M.
    Bassez, G.
    Stojkovic, T.
    Fayssoil, A.
    Laforet, P.
    Behin, A.
    Meune, C.
    Eymard, B.
    Duboc, D.
    EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 2016, 46 : 22 - 22