4
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      Osteomalacic myopathy.

      Endocrinologia japonica
      Adolescent, Female, Humans, Muscles, ultrastructure, Muscular Diseases, pathology, Necrosis, Osteomalacia

      Read this article at

      ScienceOpenPublisherPubMed
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Muscles from two cases of osteomalacia were studied histochemically and electron-microscopically. Histopathological finding were common in these two cases. There are (1) myopathic changes such as scattered muscle fiber atrophy, necrosis, and internal uuclei, (2) derangement of intermyofibrillar network. and (3) type II fiber atrophy. Electron-microscopical finding corresponded well with light microscopical findings. These are distinct pathological features and deserves to be called osteomalacic myopathy. As the pathogenetic mechanism of this myopathy, phosphate depletion in the muscle cells resulting in disturbed glycolysis, and decreased vitamin D effects on muscle cells resulting in diminished calcium uptake by sarcoplasmic reticulum, are considered to be the most important two factors.

          Related collections

          Author and article information

          Journal
          467350
          10.1507/endocrj1954.26.Supplement_65

          Chemistry
          Adolescent,Female,Humans,Muscles,ultrastructure,Muscular Diseases,pathology,Necrosis,Osteomalacia
          Chemistry
          Adolescent, Female, Humans, Muscles, ultrastructure, Muscular Diseases, pathology, Necrosis, Osteomalacia

          Comments

          Comment on this article