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Clinical significance of incidentally discovered renal cysts in pediatric patients
Ariel Botwin1, Teerasak Phewplung1,2, Kaiming Wu1
1Department of Radiology, Massachusetts General Hospital and Harvard Medical School, 55 Fruit Street, Boston, MA, 02114, USA.
Insights
Pediatric renal cysts can indicate autosomal dominant polycystic kidney disease (ADPKD). Imaging features like multiple or bilateral cysts, large size, and growth on follow-up suggest higher ADPKD risk, warranting further evaluation.
Area of Science:
- Pediatric Nephrology
- Radiology
- Medical Genetics
Background:
- Renal cysts are occasionally found incidentally in children.
- Autosomal dominant polycystic kidney disease (ADPKD) is a genetic disorder causing cyst development in the kidneys.
- Determining the significance of incidental renal cysts in pediatric patients is crucial for early ADPKD diagnosis.
Purpose of the Study:
- To assess the clinical importance of incidentally discovered renal cysts in pediatric patients.
- To identify imaging characteristics that predict the presence of autosomal dominant polycystic kidney disease (ADPKD).
Main Methods:
- Retrospective analysis of radiology reports from 2000-2016.
- Inclusion criteria: patients <18 years with renal cysts and ≥1-year follow-up imaging.
- Exclusion criteria: cysts with clear solid mass components.
Main Results:
- 84 pediatric patients with renal cysts were identified; 76 had incidentally discovered cysts.
- ADPKD was diagnosed in 7.9% of incidentally discovered cysts versus 100% in those with a family history.
- Increased cyst size, multiplicity, bilaterality, and growth on follow-up imaging were associated with higher ADPKD incidence.
Conclusions:
- Incidental renal cysts in children carry a risk of underlying autosomal dominant polycystic kidney disease (ADPKD).
- Imaging predictors such as bilaterality, multiplicity, large size, and size increase on follow-up suggest elevated ADPKD risk.
- These findings underscore the need for diagnostic evaluation when such imaging features are present.
Purpose:
To determine the clinical significance of incidentally discovered renal cysts in pediatric patients and identify imaging predictors of autosomal dominant polycystic kidney disease (ADPKD).
Methods:
A retrospective search of radiology reports from 2000 to 2016 was performed to identify patients < 18 years old with an imaging exam identifying at least one renal cyst and a ≥ 1-year follow-up renal imaging exam for cyst evaluation and/or diagnosis of ADPKD. Cysts with clear solid mass components were excluded.
Results:
84 pediatric patients with renal cysts were identified (mean age, 9.5 years), including 76 patients with incidentally discovered cysts and 8 patients with cysts identified from screening for ADPKD family history. Among the incidentally discovered cyst group, 7.9% were found to have ADPKD compared with 100% of patients with cysts and ADPKD family history. Maximum cyst diameter was significantly increased in patients with ADPKD compared to patients without ADPKD (22.0 mm vs 12.7 mm; P < 0.001, Fisher's Exact test). Multiple cysts or bilateral cysts were imaging features associated with a significantly higher (P < 0.01) incidence of ADPKD, both for the entire study population and the incidentally discovered cyst group. An increase in cyst size on the follow-up study was associated with higher incidence of ADPKD (P < 0.05). No malignancies were identified.
Conclusions:
Incidentally discovered renal cysts in pediatric patients are associated with a small but non-zero risk of ADPKD. Among cyst characteristics, bilaterality, multiplicity, large size, and increased size on follow-up imaging were associated with a statistically significant elevation of ADPKD risk, and should prompt diagnostic evaluation.
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