Renal Biopsy Interpretation Primer
Educational module for kidney biopsy interpretation and diagnostic reasoning
Light Microscopy (LM)
Mesangial proliferation, IgA deposits
Immunofluorescence (IF)
IgA (dominant), C3
Electron Microscopy (EM)
Mesangial electron-dense deposits
Clinical Presentation
Hematuria (gross or microscopic), proteinuria, normal complement
๐ก Diagnostic Pearl
Most common primary GN worldwide; IgA-dominant on IF is diagnostic
Light Microscopy (LM)
Endocapillary proliferation, 'starry sky' appearance
Immunofluorescence (IF)
IgG, C3 (C3 dominant), C1q
Electron Microscopy (EM)
Subepithelial 'humps' (pathognomonic)
Clinical Presentation
Hematuria, RBC casts, hypertension, low C3, normal C4
๐ก Diagnostic Pearl
Subepithelial humps on EM are pathognomonic; C3 returns to normal in weeks
Light Microscopy (LM)
Necrotizing GN with crescent formation, minimal immune deposits
Immunofluorescence (IF)
ANCA (MPO or PR3), minimal Ig
Electron Microscopy (EM)
Sparse or absent deposits (pauci-immune)
Clinical Presentation
Rapidly progressive GN, systemic vasculitis, positive ANCA
๐ก Diagnostic Pearl
Pauci-immune pattern on IF; ANCA serology confirms diagnosis
Light Microscopy (LM)
Necrotizing GN with crescent formation
Immunofluorescence (IF)
IgG linear along GBM (pathognomonic)
Electron Microscopy (EM)
Electron-dense deposits along GBM
Clinical Presentation
Rapidly progressive GN, possible pulmonary hemorrhage (Goodpasture)
๐ก Diagnostic Pearl
Linear IgG on IF is diagnostic; anti-GBM serology confirms
Light Microscopy (LM)
Thickened GBM, 'spike and dome' appearance
Immunofluorescence (IF)
IgG, C3 (IgG dominant)
Electron Microscopy (EM)
Subepithelial electron-dense deposits, 'spike and dome'
Clinical Presentation
Heavy proteinuria, nephrotic syndrome, normal complement, normal creatinine
๐ก Diagnostic Pearl
Spikes and domes on EM are diagnostic; check PLA2R and THSD7A antibodies
Light Microscopy (LM)
Focal segmental sclerosis, hyalinosis
Immunofluorescence (IF)
IgM, C3 (non-specific)
Electron Microscopy (EM)
Foot process effacement
Clinical Presentation
Heavy proteinuria, nephrotic syndrome, hematuria, hypertension
๐ก Diagnostic Pearl
Podocyte injury; check for secondary causes (HIV, heroin, obesity)
Light Microscopy (LM)
Normal glomeruli on light microscopy
Immunofluorescence (IF)
Negative or trace (non-specific)
Electron Microscopy (EM)
Foot process effacement (only finding)
Clinical Presentation
Pure nephrotic syndrome, normal creatinine, normal complement, selective proteinuria
๐ก Diagnostic Pearl
EM shows foot process effacement; most common cause of nephrotic syndrome in children
Light Microscopy (LM)
Mesangial proliferation, GBM duplication ('tram-track')
Immunofluorescence (IF)
C3 (dominant), IgG, IgM
Electron Microscopy (EM)
Subendothelial deposits, GBM duplication
Clinical Presentation
Hematuria, proteinuria, low C3, normal C4
๐ก Diagnostic Pearl
C3-dominant pattern; check for C3 nephrotic factor, hepatitis C
Light Microscopy (LM)
Variable (Class I-VI); 'wire loop' lesions, hyaline thrombi
Immunofluorescence (IF)
IgG, IgA, IgM, C1q, C3 ('full house')
Electron Microscopy (EM)
Subendothelial and subepithelial deposits
Clinical Presentation
Hematuria, proteinuria, low C3/C4, positive ANA/anti-dsDNA
๐ก Diagnostic Pearl
'Full house' IF pattern is highly specific; classify by WHO class
Light Microscopy (LM)
Tubular epithelial cell necrosis, loss of brush border
Immunofluorescence (IF)
Negative or non-specific
Electron Microscopy (EM)
Mitochondrial swelling, loss of brush border
Clinical Presentation
Acute rise in creatinine, FENa >2%, muddy brown casts
๐ก Diagnostic Pearl
Most common cause of intrinsic AKI; usually reversible
Light Microscopy (LM)
Interstitial edema, infiltration with lymphocytes
Immunofluorescence (IF)
IgG, IgM (variable)
Electron Microscopy (EM)
No specific findings
Clinical Presentation
Drug-induced (NSAIDs, antibiotics), fever, rash, eosinophiluria
๐ก Diagnostic Pearl
Classic triad: fever, rash, eosinophiluria; discontinue offending drug
Light Microscopy (LM)
Arteriolar necrosis, fibrinoid necrosis, RBC fragmentation
Immunofluorescence (IF)
Fibrin deposits
Electron Microscopy (EM)
Endothelial swelling, RBC fragmentation
Clinical Presentation
Microangiopathic hemolytic anemia, thrombocytopenia, AKI (HUS/TTP triad)
๐ก Diagnostic Pearl
Check ADAMTS13 (deficient in TTP); Shiga toxin in HUS
Light Microscopy (LM)
Arteriolar hyalinosis, glomerular sclerosis
Immunofluorescence (IF)
Negative or non-specific
Electron Microscopy (EM)
Arteriolar hyalinosis
Clinical Presentation
Chronic HTN, proteinuria <1 g/day, normal complement
๐ก Diagnostic Pearl
Diagnosis of exclusion; requires clinical correlation with HTN history
Light Microscopy (LM)
Amorphous deposits in glomeruli (Congo red positive, apple-green birefringence)
Immunofluorescence (IF)
Amyloid (light chain restricted)
Electron Microscopy (EM)
Fibrils (7-10 nm diameter)
Clinical Presentation
Heavy proteinuria, nephrotic syndrome, systemic amyloidosis
๐ก Diagnostic Pearl
Congo red stain with apple-green birefringence is diagnostic
Educational Disclaimer: This tool is for educational purposes only. Kidney biopsy interpretation requires expert pathology review. Always correlate biopsy findings with clinical presentation, serologies, and imaging. This primer is not a substitute for professional pathology interpretation.
Sign In Required
Please sign in or register to access this clinical tool