Glomerulonephritis: Difference between revisions
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==Background== | ==Background== | ||
* | *Glomerulonephritis (GN) = inflammation of the glomeruli, characterized by hematuria, proteinuria, and often RBC casts | ||
*Presents as '''nephritic syndrome''': hematuria, hypertension, edema, oliguria, mild-moderate proteinuria, elevated creatinine | |||
*Distinguished from nephrotic syndrome (massive proteinuria >3.5g/day, hypoalbuminemia, edema, hyperlipidemia) | |||
*Most common cause in children: '''post-streptococcal GN''' (typically self-limited) | |||
*In adults: IgA nephropathy is most common worldwide | |||
{{Glomerulonephritis causes}} | {{Glomerulonephritis causes}} | ||
==Clinical | ==Clinical Features== | ||
* | *Cola/tea-colored urine (glomerular hematuria) | ||
**Recent URI or skin infection ( | *Periorbital or peripheral edema | ||
* | *Hypertension (often the presenting finding) | ||
* | *Oliguria | ||
* | *Recent URI or skin infection 1-3 weeks prior (post-streptococcal) | ||
*Rash + arthralgia (HSP/IgA vasculitis, [[SLE]]) | |||
*Fever + bloody diarrhea → anemia + thrombocytopenia (consider [[hemolytic uremic syndrome]]) | |||
*Hemoptysis + renal failure (pulmonary-renal syndrome: Goodpasture, granulomatosis with polyangiitis) | |||
==Differential Diagnosis== | ==Differential Diagnosis== | ||
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==Evaluation== | ==Evaluation== | ||
*'''[[Urinalysis]]''': hematuria, proteinuria, '''RBC casts''' (pathognomonic for GN) | |||
*[[Urinalysis]] | *[[BMP]]: creatinine, BUN, electrolytes (hyperkalemia from renal failure) | ||
* | *[[CBC]]: anemia (HUS, chronic disease), thrombocytopenia (HUS/TTP, SLE) | ||
* | *Albumin (reduced in nephrotic features) | ||
*Albumin ( | *'''Complement levels''': low C3 (post-strep GN, MPGN, lupus), low C3 + C4 (lupus) | ||
*C3, C4, | *ASO titer, anti-DNase B (post-streptococcal) | ||
*ANA, anti-dsDNA (lupus nephritis) | |||
*ANCA (vasculitis) | |||
*[[ | *Anti-GBM antibodies (Goodpasture) | ||
*Peripheral smear if HUS suspected (schistocytes) | |||
*[[CXR]] if pulmonary-renal syndrome suspected | |||
==Management== | ==Management== | ||
* | *'''Hypertension control''': most important acute intervention — risk of hypertensive encephalopathy/seizures | ||
*Fluid/sodium restriction for edema and volume overload | |||
*Diuretics ([[furosemide]]) for significant edema or pulmonary congestion | |||
*Treat hyperkalemia if present | |||
*'''Do not delay empiric treatment''' for rapidly progressive GN (RPGN) — high-dose IV corticosteroids while awaiting biopsy results | |||
*Nephrology consultation for all suspected GN | |||
*Specific therapy depends on etiology (immunosuppression, plasmapheresis for Goodpasture/ANCA, supportive care for post-strep) | |||
==Disposition== | ==Disposition== | ||
* | *Admit: significant renal impairment, severe hypertension, pulmonary edema, suspected RPGN, HUS | ||
*Discharge: mild post-strep GN with controlled BP and stable renal function — close nephrology follow-up within 24-48 hours | |||
*Return precautions: decreased urine output, swelling, headache, visual changes, blood in urine | |||
==See Also== | |||
*[[Hematuria]] | |||
*[[Hematuria (peds)]] | |||
*[[Nephrotic syndrome]] | |||
*[[Hemolytic uremic syndrome]] | |||
==References== | ==References== | ||
Revision as of 00:34, 21 March 2026
Background
- Glomerulonephritis (GN) = inflammation of the glomeruli, characterized by hematuria, proteinuria, and often RBC casts
- Presents as nephritic syndrome: hematuria, hypertension, edema, oliguria, mild-moderate proteinuria, elevated creatinine
- Distinguished from nephrotic syndrome (massive proteinuria >3.5g/day, hypoalbuminemia, edema, hyperlipidemia)
- Most common cause in children: post-streptococcal GN (typically self-limited)
- In adults: IgA nephropathy is most common worldwide
Causes of Glomerulonephritis
- Poststreptococcal glomerulonephritis
- Hemolytic-uremic syndrome
- Henoch-Schonlein purpura
- IgA nephropathy
- Lupus nephritis
- Alport syndrome
- Goodpasture syndrome
- Paraneoplastic
Clinical Features
- Cola/tea-colored urine (glomerular hematuria)
- Periorbital or peripheral edema
- Hypertension (often the presenting finding)
- Oliguria
- Recent URI or skin infection 1-3 weeks prior (post-streptococcal)
- Rash + arthralgia (HSP/IgA vasculitis, SLE)
- Fever + bloody diarrhea → anemia + thrombocytopenia (consider hemolytic uremic syndrome)
- Hemoptysis + renal failure (pulmonary-renal syndrome: Goodpasture, granulomatosis with polyangiitis)
Differential Diagnosis
Hematuria
Sources of hematuria.
- Urologic (lower tract)
- Any location
- Iatrogenic/postprocedure
- GU trauma
- Infection
- Kidney stone
- Erosion or mechanical obstruction by tumor
- Ureter(s)
- Dilatation of stricture
- Bladder
- Transitional cell carcinoma
- Vascular lesions or malformations
- Chemical or radiation cystitis
- Prostate
- Benign prostatic hypertrophy
- Prostatitis
- Urethra
- Stricture
- Diverticulosis
- Foreign body
- Endometriosis (cyclic hematuria with menstrual pain)
- Any location
- Renal (upper tract)
- Glomerular
- Glomerulonephritis
- IgA nephropathy (Berger disease)
- Lupus nephritis
- Hereditary nephritis (Alport syndrome)
- Toxemia of pregnancy
- Serum sickness
- Erythema multiforme
- Nonglomerular
- Interstitial nephritis
- Pyelonephritis
- Papillary necrosis: sickle cell disease, diabetes, NSAID use
- Vascular: arteriovenous malformations, emboli, aortocaval fistula
- Malignancy
- Polycystic kidney disease
- Medullary sponge disease
- Tuberculosis
- Renal trauma
- Glomerular
- Hematologic
- Primary coagulopathy (e.g., hemophilia)
- Pharmacologic anticoagulation
- Sickle cell disease
- Myoglobinuria - positive blood, no RBCs: rhabdomyolysis
- Hemoglobinuria - positive blood, no RBCs
- Miscellaneous
- Eroding abdominal aortic aneurysm
- Malignant hypertension
- Loin pain–hematuria syndrome
- Renal vein thrombosis
- Exercise-induced hematuria
- Cantharidin (Spanish fly) poisoning
- Stings/bites by insects/reptiles having venom with anticoagulant properties
- Schistosomiasis
- Sickle Cell Trait
Evaluation
- Urinalysis: hematuria, proteinuria, RBC casts (pathognomonic for GN)
- BMP: creatinine, BUN, electrolytes (hyperkalemia from renal failure)
- CBC: anemia (HUS, chronic disease), thrombocytopenia (HUS/TTP, SLE)
- Albumin (reduced in nephrotic features)
- Complement levels: low C3 (post-strep GN, MPGN, lupus), low C3 + C4 (lupus)
- ASO titer, anti-DNase B (post-streptococcal)
- ANA, anti-dsDNA (lupus nephritis)
- ANCA (vasculitis)
- Anti-GBM antibodies (Goodpasture)
- Peripheral smear if HUS suspected (schistocytes)
- CXR if pulmonary-renal syndrome suspected
Management
- Hypertension control: most important acute intervention — risk of hypertensive encephalopathy/seizures
- Fluid/sodium restriction for edema and volume overload
- Diuretics (furosemide) for significant edema or pulmonary congestion
- Treat hyperkalemia if present
- Do not delay empiric treatment for rapidly progressive GN (RPGN) — high-dose IV corticosteroids while awaiting biopsy results
- Nephrology consultation for all suspected GN
- Specific therapy depends on etiology (immunosuppression, plasmapheresis for Goodpasture/ANCA, supportive care for post-strep)
Disposition
- Admit: significant renal impairment, severe hypertension, pulmonary edema, suspected RPGN, HUS
- Discharge: mild post-strep GN with controlled BP and stable renal function — close nephrology follow-up within 24-48 hours
- Return precautions: decreased urine output, swelling, headache, visual changes, blood in urine
