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Published on: June 23, 2015
Multicystic dysplastic kidney: four-year evaluation
Berna Aytaç1, Ibrahim Sehıtoğlu, Hakan Vuruskan
1Department of Pathology Uludağ University, Faculty of Medicine, Bursa, Turkey. berbun@gmail.com
Insights
Multicystic dysplastic kidney (MCDK) in children can present with other urinary tract anomalies. Surgical removal of MCDK is a management option due to potential risks, though a conservative approach is also considered.
Area of Science:
- Pediatric Nephrology
- Urology
- Developmental Biology
Background:
- Multicystic dysplastic kidney (MCDK) is a common congenital kidney abnormality in children.
- MCDK can be associated with other urinary tract anomalies, including vesicoureteral reflux and ureteropelvic junction obstruction.
Purpose of the Study:
- To review the pathogenesis, diagnosis, associated anomalies, and management outcomes of MCDK in pediatric patients.
- To evaluate the results of surgical management (nephrectomy) for unilateral MCDK.
Main Methods:
- Retrospective review of 20 children with unilateral MCDK treated between January 2005 and December 2009.
- Analysis of patient characteristics, pathology findings, associated urinary tract anomalies, and management outcomes.
- All patients underwent nephrectomy for MCDK.
Main Results:
- Associated urinary tract anomalies identified included vesicoureteral reflux (15%), ureteropelvic junction obstruction (15%), and contralateral duplex system (5%).
- All children maintained normal blood pressure, serum urea, creatinine, and urinalysis during a mean follow-up of 35 months.
- Nephrectomy was performed in all cases.
Conclusions:
- While a conservative approach for MCDK is sometimes advocated, surgical removal is a viable option.
- Considerations for surgical management include risks of hypertension, mass effect, potential malignancy, and costs associated with monitoring.
Objective:
Multicystic dysplastic kidney is a relatively common developmental abnormality in infants and children. Additional abnormalities like vesicoureteral reflux, ureteropelvic junction obstruction, and ureterovesical junction obstruction may accompany multicystic dysplastic kidney. In this article, we reviewed the pathogenesis, diagnosis, associated urinary tract anomalies and results of management of multicystic dysplastic kidney in the light of the literature.
Material And Method:
We retrospectively assessed 20 children with unilateral multicystic dysplastic kidney between January 2005 and December 2009. Mean duration of follow-up was 35 ± 8.7 months. All children with multicystic dysplastic kidney underwent nephrectomy. Patient characteristics, the pathology findings, associated urinary tract anomalies and results of management were reviewed.
Results:
Abdominal ultrasound, voiding cystourethrography and renal scintigraphy revealed vesicoureteral reflux in 3 (15%) children, ureteropelvic junction obstruction in 3 (15%) children, and a duplex system in the contralateral kidney in 1 (5%) child. Blood pressure values, serum urea, creatinine and urinalysis were within normal range in all children during follow-up.
Conclusion:
A conservative approach to children with multicystic dysplastic kidney has been advocated, but surgical removal is also another management modality on the basis of risk of hypertension, mass effect, potential for malignant change, and cost of repeated ultrasound examination.
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