Histopathological changes of myocytes in restrictive cardiomyopathy

Med Mol Morphol. 2021 Sep;54(3):289-295. doi: 10.1007/s00795-021-00293-7. Epub 2021 May 31.

Abstract

Restrictive cardiomyopathy (RCM) is a rare primary myocardial disease, and its pathological features are yet to be determined. Restrictive cardiomyopathy with MHY7 mutation was diagnosed in a 65-year-old Japanese woman. Electron microscopy of a myocardial biopsy revealed electron-dense materials resulting from focal myocyte degeneration and necrosis as well as tubular structures and pseudo-inclusion bodies in some nuclei. These features may be associated with the pathogenesis of RCM.

Keywords: Biopsy; Myocardial necrosis; Pathology.

MeSH terms

  • Aged
  • Biopsy
  • Cardiac Myosins / genetics*
  • Cardiomyopathy, Restrictive / genetics
  • Cardiomyopathy, Restrictive / metabolism
  • Cardiomyopathy, Restrictive / pathology*
  • Female
  • Humans
  • Muscle Cells / pathology*
  • Muscle Cells / ultrastructure
  • Mutation, Missense*
  • Myosin Heavy Chains / genetics*
  • Pedigree

Substances

  • MYH7 protein, human
  • Cardiac Myosins
  • Myosin Heavy Chains