Urology

Polycystic Kidney Disease

다낭성신증

Autosomal dominant (ADPKD) bilateral renal cysts

Written and edited by Dr. Kwang Lee, D.C., L.Ac. · Updated 2026-10-04

How common: Common
Typical age: Variable age

What is it?

Core pathophysiology of Polycystic Kidney Disease.

Commonly affected: 신장 전체 양측

How it develops

TriggerTriggering factor for Polycystic Kidney Disease
Local changeSpecific changes in 신장 전체 양측
ManifestationCharacteristic clinical features appear
CourseCourse depends on treatment

Symptoms

Characteristic symptomsClassic features of Polycystic Kidney Disease
Voiding/pain/hematuriaVaries by patient
Systemic symptomsWith progression

How it is examined

Physical examIdentify affected region
Urine/blood labsUA, renal function, PSA as appropriate

Imaging

Renal ultrasound or CT urography is standard.

Lesion-specific imaging findings

MRI or cystoscopy if indicated.

Adjunctive findings

Non-surgical care

PharmacotherapyTargeted medications
Lifestyle/hydration2 L/day fluids, regular voiding
SurveillanceRegular follow-up

Conservative options are generally tried first. Medications listed here can have side effects — discuss them with your prescriber.

When surgery is considered

Medical failure or complications

Procedures that may be discussed

Endoscopic procedure
Surgical treatment

Outlook

Good with appropriate treatment.