Peripheral Nerve Hyperexcitability - Cramp-Fasciculation Syndrome, Neuromyotonia and Morvan's Syndrome

被引:1
作者
Loescher, W. N. [1 ]
Cetin, H. [2 ]
Schulte-Mattler, W. J. [3 ]
Wanschitz, J. V. [1 ]
机构
[1] Univ Innsbruck, Univ Klin Neurol Med, A-6020 Innsbruck, Austria
[2] Univ Vienna, Univ Klin Neurol Med, A-1010 Vienna, Austria
[3] Univ Regensburg, Neurol Klin & Poliklin, D-93053 Regensburg, Germany
关键词
VGKC; paraneoplastic; myokymia; STIFF-PERSON SYNDROME; ACQUIRED NEUROMYOTONIA; K+ CHANNELS; ANTIBODIES; STIMULATION; DIAGNOSIS; CASPR2;
D O I
10.1055/s-0034-1383563
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Syndromes of peripheral nerve hyperexcitability represent a group of rare syndromes with distinct clinical and electrophysiological features. The mildest form, the cramp-fasciculation syndrome (CFS) is characterised by muscle cramps and fasciculations which are also seen on electromyographic recordings (EMG). In neuromyotonia (NMT) patients complain about cramps, fasciculations, muscle stiffness, paraesthesia and increased sweating. EMG shows typical high-frequency neuromyotonic discharges, doublets, triplets and multiplets. Features of Morvan's syndrome are neuromyotonia, dysautonomia and behavioural and cognitive changes. Antibodies against proteins which interact with voltage-gated potassium channels (Contactin-2, CASPR-2 und LGI-1) are found in up to 25, 50 and 90 % in patients with CFS, NMT and Morvan's syndrome. NMT and Morvan's syndrome can occur as paraneoplastic syndromes associated with thymoma and small-cell lung cancer. Paraneoplastic hyperexcitability disorders can respond to successful treatment of the tumour, autoimmune forms may respond to plasma exchange or intravenous immunoglobulins. Sodium channel blocking agents, e. g., carbamazepine, are used as symptomatic treatment.
引用
收藏
页码:201 / 206
页数:6
相关论文
共 34 条
  • [1] GLYCINE RECEPTOR ANTIBODIES IN STIFF-PERSON SYNDROME AND OTHER GAD-POSITIVE CNS DISORDERS
    Alexopoulos, Harry
    Akrivou, Sofia
    Dalakas, Marinos C.
    [J]. NEUROLOGY, 2013, 81 (22) : 1962 - 1964
  • [2] The origin of spontaneous discharges in acquired neuromyotonia.: A Macro EMG study
    Arimura, K
    Arimura, Y
    Ng, A
    Uehara, A
    Nakae, M
    Osame, M
    Stålberg, E
    [J]. CLINICAL NEUROPHYSIOLOGY, 2005, 116 (08) : 1835 - 1839
  • [3] Repetitive nerve stimulation for the evaluation of peripheral nerve hyperexcitability
    Benatar, M
    Chapman, KM
    Rutkove, SB
    [J]. JOURNAL OF THE NEUROLOGICAL SCIENCES, 2004, 221 (1-2) : 47 - 52
  • [4] Defining Normal Duration for Afterdischarges With Repetitive Nerve Stimulation: A Pilot Study
    Bodkin, Cynthia L.
    Kennelly, Kathleen D.
    Boylan, Kevin B.
    Crook, Julia E.
    Heckman, Michael G.
    Rubin, Devon I.
    [J]. JOURNAL OF CLINICAL NEUROPHYSIOLOGY, 2009, 26 (01) : 45 - 49
  • [5] NEEDLE ELECTROMYOGRAPHY
    Daube, Jasper R.
    Rubin, Devon I.
    [J]. MUSCLE & NERVE, 2009, 39 (02) : 244 - 270
  • [6] Fasciculation-cramp syndrome preceding anterior horn cell disease: an intermediate syndrome?
    de Carvalho, Mamede
    Swash, Michael
    [J]. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2011, 82 (04) : 459 - 461
  • [7] Autoimmune mediated neuromuscular junction defects
    Farrugia, Maria Elena
    Vincent, Angela
    [J]. CURRENT OPINION IN NEUROLOGY, 2010, 23 (05) : 489 - 495
  • [8] THE SYNDROME OF CONTINUOUS MUSCLE-FIBER ACTIVITY FOLLOWING GOLD THERAPY
    GRISOLD, W
    MAMOLI, B
    [J]. JOURNAL OF NEUROLOGY, 1984, 231 (05) : 244 - 249
  • [9] Myokymia and neuromyotonia 2004
    Gutmann, L
    Gutmann, L
    [J]. JOURNAL OF NEUROLOGY, 2004, 251 (02) : 138 - 142
  • [10] Accuracy of repetitive nerve stimulation for diagnosis of the cramp-fasciculation syndrome
    Harrison, Taylor B.
    Benatar, Michael
    [J]. MUSCLE & NERVE, 2007, 35 (06) : 776 - 780