Slowly Progressive ANCA-associated Glomerulonephritis with Strong Mesangial MPO Deposits Following a Diagnosis of Interstitial Lung Disease

  • Anzai Hitoshi
    Division of Nephrology, Department of Internal Medicine, Teikyo University School of Medicine, Japan
  • Suzuki Yuki
    Division of Respiratory Medicine and Allergology, Department of Internal Medicine, Teikyo University School of Medicine, Japan
  • Ueno Masaki
    Division of Nephrology, Department of Internal Medicine, Teikyo University School of Medicine, Japan
  • Asakawa Shinichiro
    Division of Nephrology, Department of Internal Medicine, Teikyo University School of Medicine, Japan
  • Nagura Michito
    Division of Nephrology, Department of Internal Medicine, Teikyo University School of Medicine, Japan
  • Arai Shigeyuki
    Division of Nephrology, Department of Internal Medicine, Teikyo University School of Medicine, Japan
  • Yamazaki Osamu
    Division of Nephrology, Department of Internal Medicine, Teikyo University School of Medicine, Japan
  • Tamura Yoshifuru
    Division of Nephrology, Department of Internal Medicine, Teikyo University School of Medicine, Japan
  • Ohashi Ryuji
    Department of Integrated Diagnostic Pathology, Nippon Medical School, Japan
  • Shibata Shigeru
    Division of Nephrology, Department of Internal Medicine, Teikyo University School of Medicine, Japan
  • Fujigaki Yoshihide
    Division of Nephrology, Department of Internal Medicine, Teikyo University School of Medicine, Japan

抄録

<p>An elderly woman showed positive conversion of myeloperoxidase (MPO)-antineutrophil cytoplasmic antibodies (ANCAs) following the diagnosis of interstitial lung disease (ILD) and glomerular hematuria and subsequently experienced slowly progressive glomerulonephritis. A kidney biopsy revealed chronic damage and necrotizing crescentic glomerulonephritis with mesangial MPO deposits. After corticosteroid treatment, the patient's urinalysis results and MPO-ANCA titers almost normalized and her renal function stabilized. This case is similar to recently reported cases of slowly progressive ANCA-associated glomerulonephritis. ILD likely triggered the production of MPO-ANCAs, and the accumulation of MPO deposits in the glomeruli may have contributed to the progression of her renal disease. </p>

収録刊行物

  • Internal Medicine

    Internal Medicine 63 (9), 1253-1260, 2024-05-01

    一般社団法人 日本内科学会

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