A case of multiple sclerosis and necrotizing autoimmune myopathy with anti-SRP antibodies

Mult Scler Relat Disord. 2018 Jan:19:118-120. doi: 10.1016/j.msard.2017.11.015. Epub 2017 Nov 23.

Abstract

Only few reports exist regarding the coexistence of multiple sclerosis (MS) and autoimmune myopathies. We describe the case of a man with a long history of undiagnosed left lower limb motor impairment who was hospitalized for subacute onset of a myopathic syndrome. In addition, neurological examination revealed sensory impairment and pyramidal signs in the left limbs. Muscle biopsy revealed a necrotizing myopathy and serum anti-signal recognition particle (SRP) antibodies were found. Brain and spinal cord MRI displayed several non-enhancing demyelinating lesions, and CSF-restricted oligoclonal bands were detected. Multimodal evoked potentials showed increased latency of central conduction. Total body PET-CT did not reveal malignancies. A final diagnosis of anti-SRP necrotizing autoimmune myopathy (NAM) and MS was made, and subsequent therapy with azathioprine resulted in a complete stability for both diseases during the follow up. To the best of our knowledge this is the first reported case of concomitant NAM and MS.

Keywords: Anti-SRP; Multiple sclerosis; Necrotizing myopathy.

Publication types

  • Case Reports

MeSH terms

  • Autoantibodies / blood*
  • Autoimmune Diseases / blood*
  • Autoimmune Diseases / pathology*
  • Corticotropin-Releasing Hormone / immunology*
  • Humans
  • Male
  • Middle Aged
  • Multiple Sclerosis*
  • Muscular Diseases / blood*
  • Muscular Diseases / pathology*
  • Necrosis / pathology
  • Urocortins / immunology*

Substances

  • Autoantibodies
  • UCN2 protein, human
  • Urocortins
  • Corticotropin-Releasing Hormone