Renal hemosiderosis and rapidly progressive glomerulonephritis associated with primary hemochromatosis


ÖZKURT S., AÇIKALIN M. F., Temiz G., Akay O. M., SOYDAN M.

RENAL FAILURE, cilt.36, sa.5, ss.814-816, 2014 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 36 Sayı: 5
  • Basım Tarihi: 2014
  • Doi Numarası: 10.3109/0886022x.2014.892391
  • Dergi Adı: RENAL FAILURE
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.814-816
  • Anahtar Kelimeler: Cardiac disorders, crescentic glomerulonephritis, diabetes mellitus, hereditary hemochromatosis, liver disease, skin pigmentation, IGA NEPHROPATHY
  • Eskişehir Osmangazi Üniversitesi Adresli: Evet

Özet

Hereditary hemochromatosis leads to the accumulation of iron in many organs including the liver, spleen and heart and results in injury and dysfunction of these organs. On the other hand, iron accumulation and functional impairment in kidney is extremely rare. We report a 61-year-old male patient with hereditary hemochromatosis, in whom the renal function was deteriorated rapidly. Renal biopsy revealed crescentic glomeruli and hemosiderin accumulation in tubular epithelial cells.