scholarly journals Percutaneous Nephrolithotomy under Ultrasound Guidance in Patients with Renal Calculi and Autosomal Dominant Polycystic Kidney Disease: A Report of 11 Cases

2017 ◽  
Vol 2017 ◽  
pp. 1-5 ◽  
Author(s):  
Xiao Wang ◽  
Xuecheng Yang ◽  
Xiulong Zhong ◽  
Zhenlin Wang ◽  
Senyao Xue ◽  
...  

Nephrolithiasis accelerates the renal failure in the patients with ADPKD. In order to evaluate the role of percutaneous nephrolithotomy in management of calculus in these patients, 11 patients with autosomal dominant polycystic kidney disease and renal stones were included in the study. Two patients had bilateral renal stones. All patients were treated by percutaneous nephrolithotomy under ultrasound guidance. 13 percutaneous nephrolithotomy procedures were performed in 1 stage by the urology team under ultrasound guidance. 5 people received second operation with flexible nephroscopy in lateral position. The success rate and morbidity and mortality of the technique and hospital stay were recorded.Results. The puncture procedure was fully successful in all cases. The renal function improved in these patients. 5 patients had moderate fever after the surgery. 5 patients received flexible nephroscopy to take out the residual calculi. 2 persons had ESWL therapy after the surgery.Conclusion. PCNL is an ideal, safe, and effective method to remove the stones from those patients with no definite increase in the risk of complication. The outcome and stone-free rate are satisfactory comparable to the PCNL in the patients without ADPKD.

2012 ◽  
Vol 2012 ◽  
pp. 1-3 ◽  
Author(s):  
Fatih Firinci ◽  
Alper Soylu ◽  
Belde Kasap Demir ◽  
Mehmet Turkmen ◽  
Salih Kavukcu

Patients with autosomal dominant polycystic kidney disease become symptomatic and are diagnosed usually at adulthood. The rate of nephrolithiasis in these patients is 5–10 times the rate in the general population, and both anatomic and metabolic abnormalities play role in the formation of renal stones. However, nephrolithiasis is rare in childhood age group. In this paper, an 11-year-old child with autosomal dominant polycystic kidney disease presenting with nephrolithiasis is discussed.


2010 ◽  
Vol 183 (1) ◽  
pp. 183-187 ◽  
Author(s):  
Eric C. Umbreit ◽  
M. Adam Childs ◽  
David E. Patterson ◽  
Vicente E. Torres ◽  
Andrew J. LeRoy ◽  
...  

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