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Mesangial lupus nephritis with associated nephrotic syndrome.
Author(s) -
Nijole Stankeviciute,
Jao W,
A. Bakir,
James P. Lash
Publication year - 1997
Publication title -
journal of the american society of nephrology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.451
H-Index - 279
eISSN - 1533-3450
pISSN - 1046-6673
DOI - 10.1681/asn.v871199
Subject(s) - lupus nephritis , nephrotic syndrome , azotemia , medicine , proteinuria , renal biopsy , systemic lupus erythematosus , mesangial proliferative glomerulonephritis , glomerulonephritis , renal function , pathology , immunology , kidney , disease
Patients with mesangial proliferative lupus glomerulonephritis (World Health Organization class II) are generally believed to have only mild to moderate proteinuria and normal renal function. However, there have been several reports of patients with mesangial lupus with nephrotic-range proteinuria. In this report, we present two additional cases and review the literature. Of seven reported cases, persistent nephrotic syndrome was observed in four, morphologic transformation occurred in three, and all but one presented with varying degrees of azotemia. These cases reinforce the concept that in systemic lupus erythematosus, laboratory findings may not correlate well with the underlying glomerular lesion, and therefore, the renal biopsy is an essential clinical tool in the approach to lupus nephritis.

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