Polycystic kidney disease: Difference between revisions

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*Hereditary disorder, autosomal dominant
*Hereditary disorder, autosomal dominant
*Accounts for ~2% of new cases of renal failure each year
*Accounts for ~2% of new cases of renal failure each year
*Mortality
 
**Cardiovascular
===Mortality===
**Infection, septicemia
*Cardiovascular
**[[Subarachnoid hemorrhage]]
*Infection, septicemia
**Uremia
*[[Subarachnoid hemorrhage]]
*Uremia


==Clinical Features==
==Clinical Features==
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**self-limited
**self-limited
**cysts are susceptible to traumatic injury
**cysts are susceptible to traumatic injury
==Differential Diagnosis==


==Evaluation==
==Evaluation==
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*CBC, BMP
*CBC, BMP
*Urinalysis +/- Urine culture
*Urinalysis +/- Urine culture
==Management==
==Disposition==
==See Also==


==References==
==References==

Revision as of 14:07, 2 October 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

Differential Diagnosis

Evaluation

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

Management

Disposition

See Also

References