Ontology highlight
ABSTRACT: Rationale
Acute renal failure developing over a short period of time with evidence of glomerular disease by urine sediment microscopy characterizes the clinical syndrome of rapidly progressive glomerulonephritis (RPGN), of which the most common causes are ANCA-associated glomerulonephritis (GN), immune-complex mediated GN and anti-GBM disease.Patient concerns
This was a middle-aged gentleman who presented with acute renal failure and a positive PR3-ANCA.Diagnosis
Renal biopsy showed an unusual combination of PR3-ANCA GN with focal crescents, monoclonal immunoglobulin deposition disease (MIDD) and mesangial IgA deposition on renal biopsy.Interventions
Serum and urine protein electrophoresis (UPEP) and immunofixation showed no detectable monoclonal paraprotein
SUBMITTER: Cassol CA
PROVIDER: S-EPMC6314724 | biostudies-literature | 2018 Dec
REPOSITORIES: biostudies-literature