Jump to content

Diffuse proliferative nephritis

From Wikipedia, the free encyclopedia
This is an old revision of this page, as edited by Nick Number (talk | contribs) at 18:11, 22 March 2016 (repaired link(s) to disambiguation pages (you can help) - SLE; fixed text formatting; removed redundant links). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

Diffuse proliferative nephritis (DPN) or glomerulonephritis (DPGN) is a type of glomerulonephritis that is the most serious form of renal lesions in SLE and is also the most common, occurring in 35% to 60% of patients. Most of the glomeruli show endothelial and mesangial proliferation affecting the entire glomerulus, leading to diffuse hypercellularity of the glomeruli, producing in some cases epithelial crescents that fill Bowman's space. When extensive, immune complexes create an overall thickening of the capillary wall, resembling rigid "wire loops" on routine light microscopy. Electron microscopy reveals electron-dense subendothelial immune complexes (between endothelium and basement membrane). Immune complexes can be visualized by staining with fluorescent antibodies directed against immunoglobulins or complement, resulting in a granular fluorescent staining pattern. In due course, glomerular injury gives rise to scarring (glomerulosclerosis). Most of these patients have hematuria with moderate to severe proteinuria, hypertension, and renal insufficiency.[1]

References

Template:Research help

  1. ^ Robbins, Stanley L.; Kumar, Vinay (2007). Robbins basic pathology. Saunders/Elsevier. p. 142. ISBN 0-8089-2366-8.{{cite book}}: CS1 maint: multiple names: authors list (link)