Behcet's disease and IgA nephropathy

被引:9
作者
Altay, Mustafa [1 ]
Secilmis, Sema [2 ]
Unverdi, Selman [2 ]
Ceri, Mevlut [2 ]
Duranay, Murat [2 ]
机构
[1] Gazi Univ, Fac Med, Dept Endocrinol & Metab, TR-06500 Ankara, Turkey
[2] Ankara Educ & Res Hosp, Dept Nephrol, Ankara, Turkey
关键词
Behcet's disease; Biopsy; Immunoglobulin A nephropathy; Proteinuria; Renal; GLOMERULONEPHRITIS; PATIENT;
D O I
10.1007/s00296-011-2051-3
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Although Beh double dagger et's disease (BD) is a kind of systemic disease, renal involvement is rare, especially IgA nephropathy (IgAN). Renal manifestations in BD range from mild urinary abnormalities to glomerulonephritis with persistent renal failure, which includes minimal change disease, proliferative glomerulonephritis, rapidly crescentic glomerulonephritis, renal amyloidosis and IgA nephropathy. Amyloidosis seems to be the most common type of renal lesion in BD, and several cases of nephrotic syndrome secondary to amyloidosis have been documented. Co-occurrence of BD and IgA nephropathy has only been reported in only few cases. We describe two patients with the rare association of BD and IgAN. We suggested that it is important to periodically perform renal function assessment in patients with BD, through urinalysis and measurement of serum creatinine for detecting any abnormality and providing an early adequate treatment.
引用
收藏
页码:2227 / 2229
页数:3
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