MRI evidence of early muscle atrophy in MuSK positive myasthenia gravis

J Neuroimaging. 2011 Jul;21(3):303-5. doi: 10.1111/j.1552-6569.2009.00456.x. Epub 2009 Dec 4.

Abstract

Muscle atrophy, particularly of facial and bulbar muscles, seems to be a relatively common long-term consequence of musclespecific tyrosine kinase-myasthenia gravis (MuSK-MG), perhaps reflecting the chronic state of disease or long-term therapy with corticosteroids. We performed magnetic resonance imaging (MRI) to assess muscle wasting in the facial and bulbar muscles in two female MuSK-MG patients, with short duration of symptoms prior to diagnosis and prior to commencement of steroid therapy. The study revealed marked atrophy of temporalis, masseters, and lingual muscles with fatty replacement. MRI evidence of early muscle atrophy in MuSK-MG may indicate that MuSK antibodies per se may predispose to muscle atrophy.

Publication types

  • Case Reports

MeSH terms

  • Female
  • Humans
  • Magnetic Resonance Imaging*
  • Middle Aged
  • Muscular Atrophy / immunology
  • Muscular Atrophy / pathology*
  • Myasthenia Gravis / immunology
  • Myasthenia Gravis / pathology*
  • Receptor Protein-Tyrosine Kinases / immunology
  • Receptors, Cholinergic / immunology
  • Young Adult

Substances

  • Receptors, Cholinergic
  • MUSK protein, human
  • Receptor Protein-Tyrosine Kinases