IgG4-related Chronic Tubulointerstitial Nephritis without Autoimmune Pancreatitis and the Time Course of Renal Function

  • Tsubata Yutaka
    Department of Internal Medicine, Niigata Prefectural Central Hospital
  • Oya Takeshi
    Department of Pathology, Niigata Prefectural Central Hospital
  • Nishi Shinichi
    Divisions of Clinical Nephrology and Rheumatology, Niigata University Graduate School of Medical and Dental Sciences
  • Narita Ichiei
    Divisions of Clinical Nephrology and Rheumatology, Niigata University Graduate School of Medical and Dental Sciences
  • Akiyama Fumihiro
    Department of Internal Medicine, Niigata Prefectural Central Hospital
  • Ajiro Junya
    Department of Internal Medicine, Niigata Prefectural Central Hospital
  • Saeki Takako
    Department of Internal Medicine, Nagaoka Red Cross Hospital

書誌事項

公開日
2010
DOI
  • 10.2169/internalmedicine.49.3787
公開者
一般社団法人 日本内科学会

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説明

We report an elderly man with chronic tubulointerstitial nephritis (TIN) showing a high serum immunoglobulin G4 (IgG4) concentration. His serum creatinine (Scr) level had gradually increased from 0.9 mg/dL to 5.6 mg/dL over 18 months. Renal biopsy showed marked IgG4-positive plasma cell infiltration in the interstitium without glomerular abnormalities and IgG4-related TIN was diagnosed. Oral prednisolone reduced his Scr and IgG4 levels immediately. The present case indicates that IgG4-related TIN can not only progress rapidly but also chronically over a long period without significant urinary abnormalities, and we should consider hidden IgG4-related TIN in cases of chronic renal insufficiency.<br>

収録刊行物

  • Internal Medicine

    Internal Medicine 49 (15), 1593-1598, 2010

    一般社団法人 日本内科学会

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