Inclusion Body Myositis: A Late Diagnosis Case Report

Reumatol Clin (Engl Ed). 2024 Nov;20(9):511-512. doi: 10.1016/j.reumae.2024.10.002. Epub 2024 Oct 28.

Abstract

Inclusion body myositis is a idiopathic inflammatory myopathy characterized by muscle weakness and dysphagia, with muscle biopsy showing inflammation and rimmed vacuoles. We present the case of a patient who was diagnosed with polymyositis but due to lack of response to treatment, a new biopsy revealed inclusion body myositis.

Keywords: Creatinine kinase; Debilidad muscular; Disfagia; Idiopathic inflammatory myopathy; Inclusion body myositis; Miopatía inflamatoria idiopática; Miositis por cuerpos de inclusión; Muscle weakness; Rimmed vacuoles; Vacuolas ribeteadas.

Publication types

  • Case Reports

MeSH terms

  • Aged
  • Delayed Diagnosis*
  • Female
  • Humans
  • Male
  • Middle Aged
  • Myositis, Inclusion Body* / diagnosis