Polycystic kidney disease: Difference between revisions

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==Clinical Features==
==Clinical Features==
*Clinical presentation typically begins in 3rd to 4th decade of life, but may be detectable in childhood
*Clinical presentation typically begins in 3rd to 4th decade of life, but may be detectable in childhood
*Pain in abdomen/flank/back is most common initial symptom. Pain can be due to:
*[[Abdominal pain]], [[flank pain]] and/or [[back pain]] is most common initial symptom.
**enlargement of cysts
**Pain due to:
**bleeding within cyst or gross hematuria with clots or perinephric hematoma
***enlargement of cysts
**urinary tract infection
***bleeding within cyst or gross [[hematuria]] with clots or perinephric hematoma
**nephrolithiasis
***[[urinary tract infection]]
*Hematuria  
***[[nephrolithiasis]]
*[[Hematuria]]
**self-limited
**self-limited
**cysts are susceptible to traumatic injury
**cysts are susceptible to traumatic injury

Revision as of 22:25, 28 September 2016

Background

  • Multisystemic and progressive disorder resulting in renal cysts and renal enlargement
  • Hereditary disorder, autosomal dominant
  • Accounts for ~2% of new cases of renal failure each year
  • Mortality

Clinical Features

Evaluation

  • US is the imaging of choice
  • CBC, BMP
  • Urinalysis +/- Urine culture

References