Glomerular |
|
• Alport syndrome |
• Thin basement membrane disease |
• IgA nephropathy |
• Pauci-immune (ANCA-related) vasculitis/anti–glomerular basement membrane disease |
|
• Henoch-Schönlein purpura |
• Systemic lupus erythematosus |
• Infection-related glomerulonephritis |
• Thrombotic microangiopathies (eg, thrombotic thrombocytopenic purpura, hemolytic uremic syndrome, scleroderma renal crisis, malignant hypertension) |
Associated with other glomerular pathology |
• Diabetic nephropathy |
• Focal segmental glomerular sclerosis |
• Minimal change disease |
• Membranous nephropathy
|
Tubular/interstitial |
• Interstitial nephritis |
• Papillary necrosis |
• Analgesic nephropathy |
• Pyelonephritis
|
Structural kidney disease–related |
• Acquired or hereditary cystic disease |
• Medullary sponge kidney |
Vascular |
• Renal vein thrombosis |
• Renal infarct/necrosis |
• Arteriovenous malformations |
• Nutcracker syndrome
|
Urothelial |
• Malignancy (involving the kidney, ureters, bladder, or prostate) |
• Nephrolithiasis |
• Nephrocalcinosis |
• Hypercalciuria |
• Strictures |
• Indwelling catheters |
• Benign prostatic hypertrophy |
• Bladder or ureteral polyps
|
Medications |
• Cyclophosphamide/ifosfamide |
• Anticoagulation associated |
Other, not rare |
• Infectious (pyelonephritis, cystitis, urethritis, prostatitis, schistosomiasis, tuberculosis, polyoma virus) |
• Rejection or trauma in a kidney transplant |
• Pelvic radiation |
• Bleeding disorders: sickle cell disease, sickle cell trait, hemophilia A or B, thrombocytopenia |
• After instrumentation of the urinary tract or trauma |
• Contamination from menstrual bleeding
|
Rare |
• Endometriosis of the urinary tract |
• Loin pain hematuria syndrome |
Urinary tract infection, Cystitis, Prostatitis, Enlarged prostate, Passage of renal calculi, infection-related glomerulonephritis (or IgA nephropathy)
Chief Complaint: Hematuria
Pivotal Assessment | Finding |
---|---|
History |