Chapter 20: Kidney Flashcards

1
Q

Subepithelial humps seen in…

A

Acute glomerulonephritis

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2
Q

Epimembranous deposits seen in…

A

Membranous glomerulopathy

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3
Q

Subendothelial deposits seen in…

A

Lupus nephritis and MPGN

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4
Q

Secondary causes of membranous glomerulopathy

A
  • drugs (penicillamine, gold, NSAIDs)
  • malignancy (lung and colon carcinoma, esp.)
  • lupus
  • infections (HCV, HBV, schisto)
  • other autoimmune disorders (thyroiditis, etc)
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5
Q

Types of FSGS

A
  • primary/idiopathic
  • associated with other diseases (HIV, sickle cell, obesity)
  • secondary to scarring from previous necrotizing lesions such as IgA nephropathy
  • as an adaptive response to loss of renal tissue
  • inherited forms of nephrotic syndrome
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6
Q

Causes of secondary MPGN

A
  • chronic immune complex disorders: HCV (with cryoglobulinemia), HCV, lupus, etc
  • A1AT deficiency
  • malignancies (CLL, lymphoma)
  • complement deficiency syndromes
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7
Q

Alport syndrome

A
  • usually X linked disorder due to abnormal chains of type IV collagen with resultant defective assembly of type IV collagen
  • hematuria with CRF, nerve deafness, cataracts, lens dislocation
  • diffuse GBM thinning
  • abundant interstitial foam cells with focal and global glomerulosclerosis developing later
  • lack of IHC staining for specific alpha 3, 4 or 5 chains; absence of alpha 5 staining also in skin biopsies from affected patients
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8
Q

Dialysis related changes in kidneys

A
  • arterial intimal thickening
  • tubulointerstitial deposition of calcium oxalate crystals
  • acquired cystic disease
  • increased incidence of adenomas and carcinomas of the kidney
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9
Q

Clinical features of HSP

A
  • purpura of extensor surfaces of arms, buttocks and legs
  • abdominal pain, vomiting, and GI bleeding
  • nonmigratory arthralgia
  • renal abnormalities including hematuria, nephritic syndrome and nephrotic syndrome
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10
Q

What is the most common cause of acute renal failure?

A

Acute kidney injury

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11
Q

Histologic features of acute kidney injury

A
  • eosinophilic tubular casts made predominantly of Tamm-Horsfall protein
  • loss of proximal tubule brush borders
  • sloughing of non-necrotic epithelial cells into the tubule lumen
  • tubular cell swelling and vacuolization
  • in ischemic cases: patchy tubular epithelial necrosis and basement membrane rupture (tubulorrhexis)
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