Glomerulopephropathies Flashcards
Nephritic Characteristics
red cells +/- white blood cells
red cell or mixed cellular casts
variable degrees of proteinuria
Nephrotic Characteristics
proteinuria > 3.5g/day
lipiduria
fatty casts
Focal nephritic
Inflammatory lesions in < ½ of glomeruli
UA shows RBCs, occasional RBC casts, mild proteinuria
Example: IgA nephropathy
Diffuse nephritic
Affects > ½ of the glomeruli
UA similar to focal, but w/ more proteinuria, also edema, HTN, and/or renal insufficiency
Example: post-streptococcal glomerulonephritis
Poststreptococcal glomerular nephritis (PSGN)
Most common cause of acute nephritis worldwide
The risk of PSGN is greatest in children between 5-12 years…seen after strep throat
Antibiotic treatment does not prevent glomerular disease
IgA Nephropathy/Berger’s Disease
Most common lesion to cause primary GN
Higher frequency in Asians and Caucasians—rare in blacks
Males
IgA Nephropathy Presentation
*Gross hematuria:
May be recurrent
Usually after URI “synpharyngitic hematuria.”
Flank Pain
Fever
Clinical predictors of progression include:
elevated serum creatinine
hypertension
and persistent protein excretion above 1000mg/day.
Henoch-Scholein Purpura (HSP)/ IgA Vasculitis
Systemic vasculitis characterized by the tissue deposition of IgA-containing immune complexes
Most common cause of vasculitis in children (90%)
HSP usually occurs between ages of 3-15
HSP Tetrad of clinical manifestations:
Palpable purpura without thrombocytopenia or coagulopathy
Arthritis/arthralgias
Abdominal pain
Renal disease (GN)
Rapidly Progressive Glomerulonephritis (RPGN) Characterized morphologically
crescent formation and clinically by progression to end-stage renal disease
RPGN Types
Anti-glomerular basement membrane (GBM/goodpastures syndrome) antibody disease of lungs and glomerulus caused by anti-GBM antibodies.
Immune complex RPGN deposition of immune complexes in the glomeruli
Pauci-immune RPGN a necrotizing glomerulonephritis and vasculitis
Interstitial Nephritis
Acute interstitial nephritis (AIN) is a renal lesion that causes a decline in creatinine clearance and is characterized by an inflammatory infiltrate in the kidney interstitium.
intrinsic renal failure.
Drugs account for 70% of cases