Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Book

Renal Cyst (Archived)

In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2026 Jan.
.
Affiliations
Free Books & Documents
Book

Renal Cyst (Archived)

David F. Sigmon et al.
Free Books & Documents

Excerpt

A renal cyst is the most common lesion of the kidney. Renal cysts are so ubiquitous that they are present in approximately 40% of the patients undergoing imaging. Cystic renal disease can be focal, multifocal, unilateral, or bilateral. Renal cysts can be acquired or the result of a congenital disease process. The acquired form is the most common.

Renal cysts can range from benign to malignant or indeterminate. A categorization system for adult renal cysts was introduced in the late 1980s, known as the Bosniak classification. It was introduced in attempts to standardize the characterization and management of renal cysts.

The terminology of congenital renal cysts has changed throughout the years, with the current characterization known as the Potter classification. The Potter classification has four categories: Type I is infantile polycystic kidney disease, Type II is multicystic dysplastic kidney disease, Type III is adult polycystic kidney disease, and Type IV is obstructive renal dysplasia.

Infantile polycystic kidney disease is also known as autosomal recessive polycystic kidney disease. ARPKD demonstrates no gender predilection with a ratio of 1:1. The age range of diagnosis is neonate to childhood, depending on the severity of the disease.

Multicystic dysplastic kidney disease is a non-inherited kidney disease that develops in utero. It is most commonly unilateral, with a higher incidence on the left side. The diagnosis is often made while still in utero or very early in a neonate.

Adult polycystic kidney disease is also known as autosomal dominant polycystic kidney disease. A patient with ADPKD has a normal appearance of the kidneys at birth and begins to develop multiple cysts bilaterally in their 20s to 30s. It is the most common inherited cause of end-stage renal failure, with more than 50% of patients requiring dialysis by the age of 60 years.

Obstructive cystic renal dysplasia results from an obstruction during development that causes scattered cysts throughout the affected kidney.

PubMed Disclaimer

Conflict of interest statement

Disclosure: David Sigmon declares no relevant financial relationships with ineligible companies.

Disclosure: Rachel Shikhman declares no relevant financial relationships with ineligible companies.

Disclosure: Jeffery Nielson declares no relevant financial relationships with ineligible companies.

References

    1. Rediger C, Guerra LA, Keays MA, Wayne C, Reddy D, Ksara S, Leonard MP. Renal cyst evolution in childhood: a contemporary observational study. J Pediatr Urol. 2019 Apr;15(2):188.e1-188.e6. - PubMed
    1. Subramanian S, Leslie SW, Ahmad T. StatPearls [Internet] StatPearls Publishing; Treasure Island (FL): 2024. Mar 3, Autosomal Recessive Polycystic Kidney Disease. - PMC - PubMed
    1. Torra R. Recent advances in the clinical management of autosomal dominant polycystic kidney disease. F1000Res. 2019;8 - PMC - PubMed
    1. Sigmon DF, Shikhman R, Nielson JL. StatPearls [Internet] StatPearls Publishing; Treasure Island (FL): 2023. Dec 27, Renal Cyst (Archived)
    1. Brown CT, Sebastião YV, McLeod DJ. Trends in surgical management of multicystic dysplastic kidney at USA children's hospitals. J Pediatr Urol. 2019 Aug;15(4):368-373. - PubMed

Publication types

LinkOut - more resources