Skip to content
Glomerulonephritis and RPGN

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 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.