Renal hemosiderosis and rapidly progressive glomerulonephritis associated with primary hemochromatosis

被引：18

作者：

Ozkurt, Sultan ^{[1
]}

Acikalin, Mustafa Fuat ^{[2
]}

Temiz, Gokhan ^{[1
]}

Akay, Olga Meltem ^{[3
]}

Soydan, Mehmet ^{[1
]}

机构：

[1] Eskisehir Osmangazi Univ, Dept Nephrol, Fac Med, TR-26000 Eskisehir, Turkey

[2] Eskisehir Osmangazi Univ, Dept Pathol, Fac Med, TR-26000 Eskisehir, Turkey

[3] Eskisehir Osmangazi Univ, Dept Hematol, Fac Med, TR-26000 Eskisehir, Turkey

来源：

RENAL FAILURE | 2014年 / 36卷 / 05期

关键词：

Cardiac disorders; crescentic glomerulonephritis; diabetes mellitus; hereditary hemochromatosis; liver disease; skin pigmentation; IGA NEPHROPATHY;

D O I：

10.3109/0886022X.2014.892391

中图分类号：

R5 [内科学]; R69 [泌尿科学（泌尿生殖系疾病）];

学科分类号：

1002 ; 100201 ;

摘要：

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.

引用

页码：814 / 816

页数：3

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