LDH-IgA COMPLEXES ASSOCIATED WITH IgA GLOMERULONEPHRITIS

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  • IIZUKA TAKASHI
    The Second Department of Internal Medicine, Gunma University School of Medicine
  • KUMAKURA HISAO
    The Second Department of Internal Medicine, Gunma University School of Medicine
  • TOMONO SHOICHI
    The Second Department of Internal Medicine, Gunma University School of Medicine
  • SUZUKI TADASHI
    The Second Department of Internal Medicine, Gunma University School of Medicine
  • MURATA KAZUHIKO
    The Second Department of Internal Medicine, Gunma University School of Medicine
  • USHIJIMA YOSHIO
    The Clinical Laboratory, Gunma University Hospital
  • ARAI MASAO
    The Clinical Laboratory, Gunma University Hospital
  • OIKE SOSUKE
    The Third Department of Internal Medicine, Gunma University School of Medicine

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Other Title
  • IgA結合性LDH-anomalyを伴ったIgA腎症の一症例
  • IgA ケツゴウセイ LDH anomaly オ トモナッタ IgA ジンショ

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Description

A 15-year-old boy was admitted to the hospital because of increased serum LDH activity and microhematuria. The gel filtration and the immunoelectrophoresis revealed the presence of high molecular LDH-IgA complex, while the diagnosis of IgA glomerulonephritis was established by renal biopsy. It was postulated that IgA abnormality might be responsible both for formation of high molecular LDH-IgA complex and development of glomerulonephritis in this case.

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