RENAL DISEASE Flashcards

1
Q
  1. Most glomerular disorders are caused by:
    A. Sudden drops in blood pressure
    B. Immunologic disorders
    C. Exposure to toxic substances
    D. Bacterial infections
A

B. Immunologic disorders

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2
Q

2 Dysmorphic RBC casts would be a significant finding with all of the following except:
A. Goodpasture syndrome
B. AGN
C. Chronic pyelonephritis
D. Henoch-Schonlein purpura

A

C. Chronic pyelonephritis

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3
Q
  1. Occasional episodes of macroscopic hematuria over periods of 20 or more years are seen in patients with:
    A. Crescentic glomerulonephritis
    B. IgA nephropathy
    C. Nephrotic syndrome
    D. GPA
A

B. IgA nephropathy

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4
Q
  1. Antiglomerular basement membrane antibody is seen with:
    A. GPA
    B. IgA nephropathy
    C. Goodpasture syndrome
    D. Diabetic nephropathy
A

C. Goodpasture syndrome

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5
Q
  1. ANCA is diagnostic for:
    A. IgA nephropathy
    B. GPA
    C. Henoch-Schonlein purpura
    D. Goodpasture syndrome
A

B. GPA

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6
Q
  1. Respiratory and renal symptoms are associated with all of the following except:
    A. IgA nephropathy
    B. GPA
    C. Henoch-Schonlein purpura
    D. Goodpasture syndrome
A

A. IgA nephropathy

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7
Q
  1. The presence of fatty casts is associated with all of the following except:
    A. Nephrotic syndrome
    B. FSGS
    C. Nephrogenic DI
    D. MCD
A

C. Nephrogenic DI

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8
Q
  1. The highest levels of proteinuria are seen with:
    A. Alport syndrome
    B. Diabetic nephropathy
    C. IgA nephropathy
    D. NS
A

D. NS

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9
Q
  1. Ischemia frequently produces:
    A. Acute renal tubular necrosis
    B. MCD
    C. Renal glycosuria
    D. Goodpasture syndrome
A

A. Acute renal tubular necrosis

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10
Q
  1. A disorder associated with polyuria and low specific gravity is:
    A. Renal glucosuria
    B. MCD
    C. Nephrogenic DI
    D. FSGS
A

C. Nephrogenic DI

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11
Q
  1. An inherited disorder producing a generalized defect in tubular reabsorption is:
    A. Alport syndrome
    B. AIN
    C. Fanconi syndrome
    D. Renal glycosuria
A

C. Fanconi syndrome

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12
Q
  1. A teenage boy who develops gout in his big toe and has a high serum uric acid should be monitored for:
    A. Fanconi syndrome
    B. Renal calculi
    C. Uromodulin-associated kidney disease
    D. Chronic interstitial nephritis
A

C. Uromodulin-associated kidney disease

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13
Q
  1. The only protein produced by the kidney is:
    A. Albumin
    B. Uromodulin
    C. Uroprotein
    D. Globulin
A

B. Uromodulin

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14
Q
  1. The presence of RTE cells and casts is an indication of:
    A. AIN
    B. CGN
    C. MCD
    D. ATN
A

D. ATN

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15
Q
  1. Differentiation between cystitis and pyelonephritis is aided by the presence of:
    A. WBC casts
    B. RBC casts
    C. Bacteria
    D. Granular casts
A

A. WBC casts

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16
Q
  1. The presence of WBCs and WBC casts with no bacteria is indicative of:
    A. Chronic pyelonephritis
    B. ATN
    C. AIN
    D. Both B and C
A

C. AIN

17
Q
  1. ESRD is characterized by all of the following except:
    A. Hypersthenuria
    B. Isosthenuria
    C. Azotemia
    D. Electrolyte imbalance
A

A. Hypersthenuria

18
Q
  1. Prerenal acute renal failure could be caused by:
    A. Massive hemorrhage
    B. ATN
    C. AIN
    D. Malignant tumors
A

A. Massive hemorrhage

19
Q
  1. The most common component of renal calculi is:
    A. Calcium oxalate
    B. Magnesium ammonium phosphate
    C. Cystine
    D. Uric acid
A

A. Calcium oxalate

20
Q
  1. Urinalysis on a patient with severe back pain being evaluated for renal calculi would be most beneficial if it showed:
    A. Heavy proteinuria
    B. Low specific gravity
    C. Uric acid crystals
    D. Microscopic hematuria
A

D. Microscopic hematuria