Glomerulonephritis: Difference between revisions

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(Expanded with concise EM-focused content: nephritic syndrome features, complement-based workup, BP management, RPGN urgency)
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==Background==
==Background==
*Characterized by [[hematuria]] and [[proteinuria]]
*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 Presentation==
==Clinical Features==
*History
*Cola/tea-colored urine (glomerular hematuria)
**Recent URI or skin infection (strep)
*Periorbital or peripheral edema
**[[Rash]], [[arthralgia]] (HSP, SLE)
*Hypertension (often the presenting finding)
**[[Fever]], [[vomiting]], [[diarrhea]] (HUS)
*Oliguria
*Often associated with hypertension
*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==
===Work-Up===
*'''[[Urinalysis]]''': hematuria, proteinuria, '''RBC casts''' (pathognomonic for GN)
*[[Urinalysis]]
*[[BMP]]: creatinine, BUN, electrolytes (hyperkalemia from renal failure)
*CBC
*[[CBC]]: anemia (HUS, chronic disease), thrombocytopenia (HUS/TTP, SLE)
*Chemistry
*Albumin (reduced in nephrotic features)
*Albumin (often reduced in acute glomerulonephritis)
*'''Complement levels''': low C3 (post-strep GN, MPGN, lupus), low C3 + C4 (lupus)
*C3, C4, ASO
*ASO titer, anti-DNase B (post-streptococcal)
 
*ANA, anti-dsDNA (lupus nephritis)
===Diagnosis===
*ANCA (vasculitis)
*[[Hematuria]], [[proteinuria]], RBC casts
*Anti-GBM antibodies (Goodpasture)
*Peripheral smear if HUS suspected (schistocytes)
*[[CXR]] if pulmonary-renal syndrome suspected


==Management==
==Management==
*Defer to nephrologist
*'''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==
*Coordinate with nephrologist
*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

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.

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

See Also

References