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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
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.
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