[PDF] Autosomal Dominant Polycystic Kidney Disease: Core Curriculum

  • What is the teaching of polycystic kidney disease?

    Polycystic kidney disease (also called PKD) causes numerous cysts to grow in the kidneys. These cysts are filled with fluid. If too many cysts grow or if they get too big, the kidneys can become damaged. PKD cysts can slowly replace much of the kidneys, reducing kidney function and leading to kidney failure.

  • What are the criteria for autosomal dominant polycystic kidney disease?

    The diagnosis of ADPKD is established by any of the following: At least 2 kidney cysts or 1 cyst in each kidney in patients younger than 30 years. At least 2 cysts in each kidney in patients aged 30-59 years old. At least 4 cysts in each kidney in patients aged 60 years or older.

  • What is the difference between ADPKD and ARPKD?

    ADPKD shows cysts of varying sizes which may show coarse calcifications and renal calculi. Cysts in ARPKD are mostly microcystic. Cysts in ADPKD can arise from anywhere along the nephron, most commonly from the collecting tube. However, cysts in ARPKD arise exclusively in the collecting tubule.

  • Polycystic Kidney Disease Treatment & Management

    Approach Considerations.Blood Pressure Control.Infectious and Other Disorders.Surgical Drainage.Consultations and Long-Term Monitoring.Diet.Activity.Show All.
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