Renal Disorders I Flashcards

1
Q

Clinical symptoms of acute kidney injury

A
  • oliguria

- elevated serum creatinine

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2
Q

Clinical signs of nephrotic syndrome

A
  • severe proteinuria
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3
Q

Clinical signs of nephritic syndrome

A
  • hematuria
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4
Q

Location of injury in acute kidney injury

A
  • proximal tubule, sometimes distal tubule
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5
Q

Location of injury in nephrotic syndrome

A
  • glomerular capillary filtration defect (podocyte defect)
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6
Q

Location of injury in nephritic syndrome

A
  • breaks in the glomerular capillary loops
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7
Q

Possible diagnoses for acute kidney injury

A
  • acute tubular necrosis
  • acute interstitial nephritis
  • acute pyelonephritis
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8
Q

Possible diagnoses for nephrotic syndrome

A
  • membranous nephropathy
  • FSGS
  • minimal change disease
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9
Q

Possible diagnoses for nephritic syndrome

A
  • acute nephritic syndrome: crescentic glomerulonephritis, lupus nephritis, post infectious glomerulonephritis
  • isolated hematuria: IgA nephropathy, alport’s disease
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10
Q

Clinical indicators of renal dysfunction

A
  • edema
  • decreased renal output
  • foamy urine: proteinuria
  • dark or red urine: hematuria (tea colored, cola colored)
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11
Q

Laboratory indicators of renal dysfunction

A
  • increased creatinine, blood urea nitrogen
  • increased protein excretion (urine dipstick, urine protein/creatinine ratio, 24 hour urine protein)
  • hematuria (urine dipstick, microscopic exam)
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12
Q

Signs of chronic kidney disease

A
  • Glomerular sclerosis
  • interstitial fibrosis
  • tubular atrophy
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13
Q

Ways to assess renal biopsy

A
  • light microscopy
  • immunofluorescence microscopy
  • electron microscopy
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14
Q

Patterns of immunofluorescence staining in glomerulus

A
  • linear capillary loop pattern
  • granular capillary loop pattern
  • mesangial pattern
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15
Q

Disease associated with linear capillary loop pattern immunofluorescence stain

A
  • Anti-GBM disease
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16
Q

Diseases associated with granular capillary loop pattern immunofluorescence stain

A
  • membranous nephropathy, lupus nephritis
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17
Q

Diseases associated with mesangial pattern immunofluorescence stain

A
  • IgA nephropathy, lupus nephritis
18
Q

Layers of basement membrane

A
  • lamina externa
  • lamina densa
  • lamina interna
19
Q

Mechanisms of glomerular injury

A
  1. immune mechanisms: immune complex mediated, T-cell mediated
  2. non immune mechanisms: structural disorders
20
Q

Disorder associated with immune complex mediated glomerular injury

A
  • membranous glomerulopathy
21
Q

Disorders associated with T-cell mediated glomerular injury

A
  • minimal change disease

- lupus nephritis

22
Q

Disorder associated with non immune glomerular injury

A
  • alport’s syndrome
23
Q

Mutation associated with alport’s syndrome

A
  • mutation in collagen type IV gene

- leads to structural weakness in basement membrane b/c it’s composed of collagen type IV

24
Q

Patient presentation and lab values seen with acute kidney injury

A
  • decreased urinary output (oliguria), and uremia (azotemia)

- labs: increased serum creatinine, and blood urea nitrogen

25
Q

Types of acute kidney injury

A
  • pre renal
  • renal
  • post renal
26
Q

Pre renal acute kidney injury causes

A
  • cardiac shock, dehydration
27
Q

Renal acute kidney injury

A
  • tubulointerstitial diseases
28
Q

Post renal acute kidney injury causes

A
  • obstructive renal stone
29
Q

Causes of acute kidney injury

A
  • acute tubular necrosis
  • acute interstitial nephritis
  • acute pyelonephritis
30
Q

Acute tubular necrosis prevelance

A
  • MOST COMMON cause of acute kidney injury
31
Q

Causes of acute tubular necrosis

A
  • injury to tubular epithelial cells

- hypovolemia, ischemia, drug toxicity

32
Q

Presentation of ATN & reversibility

A
  • oliguria

- reversible

33
Q

Key features of ATN

A
  • tubular dilation and flattening of tubular epithelial cells
  • necrotic debris in tubular lumen
34
Q

Acute interstitial nephritis key featurs

A
  • interstitial inflammation and tubulitis (lymphocytes in interstitium and in the tubule)
  • EOSINOPHILS = drug induced (if eosinophils are present)
35
Q

Acute pyelonephritis causes

A
  • infections of pelvicalyceal system, and renal parenchyma
36
Q

Presentation of acute pyelonephritis

A
  • pain in cost-vertebral angle + other signs of infections
37
Q

Diagnosis of acute pyelonephritis

A
  • pus (WBC) casts

- positive urine culture

38
Q

Key features of acute pyelonephritis

A
  • similar to interstitial nephritis but inflammatory cells are NEUTROPHILS
  • neutrophilic infiltrates and neutrophil casts in tubules are characteristic
39
Q

Prognosis of acute pyelonephritis

A
  • benign course if treated, symptoms disappear after treatment with antibiotics
40
Q

Chronic pyelonephritis course

A
  • may have insidious onset or a history of recurrent acute pyelonephritis
  • gradual loss of renal function
  • results in scarred kidney with chronic inflammation
41
Q

Key features of chronic pyelonephritis

A
  • scarred kidneys, chronic inflammation

- severe tubular atrophy, “thyroidization” of the kidney

42
Q

Three clinical renal syndromes

A
  • acute kidney injury
  • nephrotic syndrome
  • nephritic syndrome