Glomerulonephritis and RPGN
Glomerulonephritis and RPGN - Practical evaluation of nephritic syndrome, complement patterns and rapidly progressive GN.
Practical orientation: GN is usually a biopsy diagnosis. In rapidly progressive presentations, do not wait passively for serology before discussing urgent biopsy and treatment.
Use first: clinical summary and algorithm.
Then: differential diagnosis, workup and management tables.
Escalate: use red flags and biopsy/urgent-care sections.
Clinical summary
GN phenotype
Inflammatory glomerular disease with hematuria, dysmorphic RBCs/RBC casts, azotemia, hypertension and variable proteinuria.
RPGN
Rapid kidney function decline over days to months; urgent diagnosis and treatment required.
Key test
Kidney biopsy plus targeted serology.
Do not delay
Severe RPGN may need empiric pulse glucocorticoids while biopsy is pending.
Algorithm
Clinical manifestations
| Finding | Meaning |
|---|---|
| Dysmorphic RBCs/acanthocytes | Glomerular hematuria. |
| RBC casts | Strongly suggests glomerular inflammation. |
| Proteinuria | Often subnephrotic, but nephrotic-range proteinuria can occur. |
| Hypertension and reduced eGFR | Common in active GN. |
Initial serologic workup
| Test group | Examples |
|---|---|
| Complement | C3, C4. |
| Autoimmune | ANA, anti-dsDNA, ANCA with MPO/PR3, anti-GBM. |
| Infection | Hepatitis B/C, HIV, blood cultures if endocarditis possible. |
| Immune-complex / paraprotein | Cryoglobulins, RF, SPEP/IFE, serum free light chains. |
Complement patterns
| Complement pattern | Consider |
|---|---|
| Low complement | Lupus nephritis, infection-related GN, cryoglobulinemic GN, C3G, MPGN, endocarditis and selected monoclonal deposit diseases. |
| Normal complement | Pauci-immune GN, anti-GBM disease, IgA nephropathy, fibrillary GN. |
Extra-renal clues
| Disease | Clues |
|---|---|
| IgA vasculitis | Palpable purpura, abdominal pain, GI bleeding, arthralgia/arthritis. |
| SLE | Fever, rash, serositis, arthritis, neuropsychiatric disease, low complement. |
| ANCA vasculitis | ENT disease, pulmonary hemorrhage/nodules, purpura, neuropathy. |
| Anti-GBM disease | Pulmonary hemorrhage, severe crescentic GN. |
| Cryoglobulinemic GN | Purpura, ulcers, neuropathy, arthralgia/myalgia. |
| Alport syndrome | Hearing loss and ocular abnormalities. |
RPGN management principles
| Step | Action |
|---|---|
| Recognize | Rapid creatinine rise plus nephritic sediment. |
| Urgent tests | Serology and kidney biopsy. |
| Empiric therapy | Pulse IV methylprednisolone can be started if severe and biopsy pending. |
| Plasma exchange | Consider in diffuse alveolar hemorrhage and selected severe anti-GBM/ANCA presentations. |
| Definitive therapy | Disease-specific immunosuppression and supportive nephroprotection. |