Please confirm topic selection

Are you sure you want to trigger topic in your Anconeus AI algorithm?

Please confirm action

You are done for today with this topic.

Would you like to start learning session with this topic items scheduled for future?

Review Question - QID 101024

In scope icon M 1 E
QID 101024 (Type "101024" in App Search)
A 7-year-old boy suffers from generalized edema. Urine protein excretion is 5.2 g over 24 hours, and serum analysis reveals hyperlipidemia. The patient responds to treatment with prednisone, and, 8 weeks later, his urine does not contain measurable protein. If a kidney biopsy had been performed while the patient’s condition was pathologic, which of the following would you expect to find upon glomerular electron microscopy?

Effacement of podocyte foot processes

88%

225/256

Subepithelial ‘spike and dome’ deposits

3%

8/256

Subepithelial humps

2%

6/256

Thin glomerular basement membrane

4%

9/256

Subendothelial thickening

1%

3/256

Select Answer to see Preferred Response

bookmode logo Review TC In New Tab

The clinical scenario describes a child suffering from minimal change disease. In minimal change disease, effacement of podocyte foot processes can be seen upon electron microscopy.

Edema, hyperlipidemia, and urine protein excretion of greater than 3.5 grams over 24 hours are cardinal features of nephrotic syndrome. Minimal change disease (lipoid nephrosis) is the most common cause of nephrotic syndrome in children aged 1-7 and is often responsive to steroid treatment. Focal segmental glomerular sclerosis is also common in children and produces nephrotic syndrome. However, the disease is less consistently responsive to steroid treatment than minimal change disease and does not produce characteristic findings upon electron microscopy.

Gibson et al. discuss management of childhood nephrotic syndrome. Complications can arise from chronic steroid use and include hypertension, obesity, and linear growth retardation. Steroid-sparing regimens also require monitoring, and can produce varied adverse effects.

Cho et al. review the pathophysiology of minimal change disease. Some data suggest T cells release a cytokine permeability factor that injures glomerular epithelial cells. Epithelial cell damage may in turn lead to albuminuria by altering polyanions, such as heparan sulfates, that form much of the charge barrier to the glomerular filtration of albumin.

Illustration A shows the three hallmarks of minimal change disease: diffuse loss of podocyte foot processes, vacuolation, and the appearance of microvilli.

Incorrect Answers:
Answer 2: Subepithelial ‘spike and dome’ deposits are characteristic of membranous glomerulonephritis.

Answer 3: Subepithelial humps are characteristic of acute proliferative glomerulonephritis, also known as acute poststreptococcal glomerulonephritis.

Answer 4: A thin glomerular basement membrane is characteristic of Alport's syndrome.

Answer 5: Subendothelial thickening is characteristic of membranoproliferative glomerulonephritis.

Bullet Summary: Effacement of podocyte foot processes is seen in minimal change disease.

ILLUSTRATIONS:
REFERENCES (2)
Authors
Rating
Please Rate Question Quality

5.0

  • star icon star icon star icon
  • star icon star icon star icon
  • star icon star icon star icon
  • star icon star icon star icon
  • star icon star icon star icon

(4)

Attach Treatment Poll
Treatment poll is required to gain more useful feedback from members.
Please enter Question Text
Please enter at least 2 unique options
Please enter at least 2 unique options
Please enter at least 2 unique options