@ Autosomal Dominent Polycystic kidney Disease.................

Hello all fellows ,

Today we talk about Polycystic kidney disease . There are two types of it.

  1. Autosomal Dominent Polycystic kidney disease (ADPCKD)

  2. Autosomal Recessive Polycystic kidney disease (ARPCKD)

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                   Pic: collected

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Clinical Symptoms :

  • Asymptomatic most patients
  • Hematuria ( Blood passing through urine )
  • Pain on Flank ( infections, any cyst rupture, kidney stone, internal bleedings )

Clinical Signs :

  • High Blood pressure (HTN)
  • Proteinuria ( Protein passing through urine)
  • Bilateral abdominal masses
  • Chronic kidney/renal disease

Other Extrarenal features :

  • Ventral and inguinal hernias
  • Cardiac valves disorders ( Mitral valve prolapse, Aortic Regurgitation )
  • Colonic diverticulosis
  • Hepatic and pancreatic cyst
  • Cerebral aneurysms

How to Diagnose:

*USG( Ultrasonogram mainly)
*CT scan( computed tomography), MRI (Magnetic resonance imaging )
shows multiple renal cysts

Treatment or Management :

  • Continuous Blood pressure and renal function follow up.
  • Hypertension control aggressively
  • ACE inhibitors for high blood pressure
  • In case of end-stage renal disease- Dialysis , renal transplant

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Until next time ……

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