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37 Cards in this Set
- Front
- Back
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alpha-5 chain of type IV collagen
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Alport syndrome
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Sensorineural hearing loss and ocular abnormalities
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Alport syndrome
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Splitting and lamellation of GBM
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Alport syndrome
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Normal renal function, normal LM and IF, microscopic hematuria
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Thin basement membrane disease
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Recurrent gross but asymptomatic hematuria following infection
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Berger's IgA nephropathy
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LM: mesangial proliferation, focal segmental endocapillary proliferation or sclerosis
IF: mesangial IgA EM: mesangial granular deposits |
Berger's IgA nephropathy
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alpha-3 chain of type IV collagen
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Goodpasture's syndrome
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LM: focal segmental fibrinoid necrosis, cresentic proliferation
IF: linear staining with IgG, C3 |
Goodpasture's syndrome
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Pauci-immune glomerulonephritis
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Wegener's granulomatosis, Churg-Strauss, polyangiitis, ANCA-related)
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Immune complex-mediated nephritis
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Lupus nephritis, Henoch-Schonlein purpura, MPGN, IgA nephropathy, postinfectious GN
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WBC casts in UA, flank pain, fever, dysuria
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Acute pyelonephritis
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Dysuria, frequency, urgency, without fever, bacteriuria and pyuria
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Acute cystitis
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Wire loops, hyaline thrombi, hematoxylin bodies
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Lupus nephritis
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Humps (subepithelial deposits)
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Acute postinfectious GN
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Tubuloreticular inclusions
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Lupus nephritis
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c-ANCA
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Wegener's granulomatosis
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p-ANCA
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Churg-Strauss syndrome
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Transmural arteritis and fibrinoid necrosis; no involvement of glomeruli
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Polyarteritis nodosa
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Systemic necrotizing vasculitis with small vessel involvement
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Wegener's granulomatosis
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Hepatitis B infection
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Polyarteritis nodosa
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Schistosomiasis
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Squamous carcinoma of the bladder
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Mesangial IgA deposits
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Henoch-Schonlein purpura
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Segmental to diffuse cortical necrosis
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Hemolytic uremic syndrome (HUS)
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Kimmelstiel-Wilson nodules
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Diabetic glomerulosclerosis
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Epithelial foot process effacement
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Minimal change disease/nil lesion
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Subendothelial humps; tram-tracks
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Membranoproliferative GN
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Membranous GN: nephrotic or nephritic?
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Nephrotic
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Membranoproliferative GN: nephrotic or nephritic?
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Nephritic
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Diffuse capillary and basement membrane thickening
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Membranous GN
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Most common cause of childhood nephrotic syndrome
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Minimal change disease
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Common cause of adult nephrotic syndrome
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Membranous GN
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von Hippel-Lindau and gene deletion in chromosome 3
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Renal cell carcinoma
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Most common renal malignancy of early childhood (ages 2-4)
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Wilms' tumor
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Most common tumor of urinary tract system
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Transitional cell carcinoma
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Thyroidization of kidney
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Chronic pyelonephritis
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WBC casts in urine
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Acute pyelonephritis
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Most common cause of acute renal failure
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Acute tubular necrosis
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