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KEY FACTS
Terminology
Imaging
Top Differential Diagnoses
Clinical Issues
Diagnostic Checklist
TERMINOLOGY
Abbreviations
- Autosomal dominant polycystic kidney disease (ADPKD)
Synonyms
- Potter classification type 3: Adult onset polycystic kidney disease
Definitions
- Most common hereditary renal cystic disease
- Progressive development of multiple enlarging, bilateral renal cysts, parenchymal replacement, and end-stage renal disease
IMAGING
General Features
Ultrasonographic Findings
Radiographic Findings
CT Findings
MR Findings
Imaging Recommendations
DIFFERENTIAL DIAGNOSIS
PATHOLOGY
General Features
Staging, Grading, & Classification
Gross Pathologic & Surgical Features
CLINICAL ISSUES
Presentation
Demographics
Natural History & Prognosis
Treatment
DIAGNOSTIC CHECKLIST
Consider
Image Interpretation Pearls
Selected References
- Nobakht N et al: Advances in autosomal dominant polycystic kidney disease: a clinical review. Kidney Med. 2(2):196-208, 2020
- Gimpel C et al: Imaging of kidney cysts and cystic kidney diseases in children: an International Working Group consensus statement. Radiology. 290(3):769-82, 2019
- Dillman JR et al: Hereditary renal cystic disorders: imaging of the kidneys and beyond. Radiographics. 37(3):924-46, 2017
- Akoh JA: Current management of autosomal dominant polycystic kidney disease. World J Nephrol. 4(4):468-79, 2015
- Avni FE et al: Imaging and classification of congenital cystic renal diseases. AJR Am J Roentgenol. 198(5):1004-13, 2012
- Katabathina VS et al: Adult renal cystic disease: a genetic, biological, and developmental primer. Radiographics. 30(6):1509-23, 2010
- Pei Y et al: Diagnosis and screening of autosomal dominant polycystic kidney disease. Adv Chronic Kidney Dis. 17(2):140-52, 2010
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Related Differential Diagnoses
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References
Tables
Tables
KEY FACTS
Terminology
Imaging
Top Differential Diagnoses
Clinical Issues
Diagnostic Checklist
TERMINOLOGY
Abbreviations
- Autosomal dominant polycystic kidney disease (ADPKD)
Synonyms
- Potter classification type 3: Adult onset polycystic kidney disease
Definitions
- Most common hereditary renal cystic disease
- Progressive development of multiple enlarging, bilateral renal cysts, parenchymal replacement, and end-stage renal disease
IMAGING
General Features
Ultrasonographic Findings
Radiographic Findings
CT Findings
MR Findings
Imaging Recommendations
DIFFERENTIAL DIAGNOSIS
PATHOLOGY
General Features
Staging, Grading, & Classification
Gross Pathologic & Surgical Features
CLINICAL ISSUES
Presentation
Demographics
Natural History & Prognosis
Treatment
DIAGNOSTIC CHECKLIST
Consider
Image Interpretation Pearls
Selected References
- Nobakht N et al: Advances in autosomal dominant polycystic kidney disease: a clinical review. Kidney Med. 2(2):196-208, 2020
- Gimpel C et al: Imaging of kidney cysts and cystic kidney diseases in children: an International Working Group consensus statement. Radiology. 290(3):769-82, 2019
- Dillman JR et al: Hereditary renal cystic disorders: imaging of the kidneys and beyond. Radiographics. 37(3):924-46, 2017
- Akoh JA: Current management of autosomal dominant polycystic kidney disease. World J Nephrol. 4(4):468-79, 2015
- Avni FE et al: Imaging and classification of congenital cystic renal diseases. AJR Am J Roentgenol. 198(5):1004-13, 2012
- Katabathina VS et al: Adult renal cystic disease: a genetic, biological, and developmental primer. Radiographics. 30(6):1509-23, 2010
- Pei Y et al: Diagnosis and screening of autosomal dominant polycystic kidney disease. Adv Chronic Kidney Dis. 17(2):140-52, 2010
