Autosomal dominant polycystic kidney disease

USG · MRI · CT

First and second year — the floor first, then every step

Bilateral enlarged kidneys replaced by cysts: diagnose by age-specific cyst counts, measure total kidney volume (it predicts progression and qualifies for therapy), and look for complications — haemorrhage, infection, stones, and liver cysts.

Orient first

  • Diagnostic ultrasound criteria depend on age and family history (unified criteria — verify).
  • Height-adjusted total kidney volume (htTKV) on MRI stratifies risk (Mayo imaging classification — verify).
  • Extrarenal: liver cysts, intracranial aneurysms (screening by family history), pancreatic cysts.

Acquire the study

  • Curvilinear probe; both kidneys in longitudinal and transverse planes.

The manoeuvre

  • Count cysts per kidney and compare with the age-specific criteria.
  • Kidney length in cm on both sides.
  • Complicated cysts: internal echoes, fluid–debris levels.
  • Liver cysts.

What confirms it

  • Bilateral cysts meeting the age-specific criteria with family history or genetics.

What licenses you to exclude it

  • Age-specific criteria allow exclusion in an at-risk adult when the cyst count is below threshold (verify).

The classic misread

  • Diagnosing ADPKD from a few simple cysts in an older adult — simple cysts increase with age.

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