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Segmental multicystic dysplasia and ureteropelvic junction obstruction in a nonduplicated kidney

✍ Scribed by Adrienne J.K. Carmack; Miguel Castellan; Marcos Perez-Brayfield; Rafael Gosalbez


Book ID
116685794
Publisher
Elsevier Science
Year
2006
Tongue
English
Weight
235 KB
Volume
41
Category
Article
ISSN
0022-3468

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✦ Synopsis


A 2-month-old child presented for evaluation of prenatal hydronephrosis. Imaging studies were consistent with a right duplex system with a dysplastic, nonfunctioning upper pole and lower pole ureteropelvic junction obstruction. We proceeded with removal of the upper pole and pyeloplasty and were surprised to find a single collecting system with a cystic, dysplastic upper pole segment and the absence of an upper pole pelvis or ureter. The rare diagnosis of a segmental multicystic dysplastic kidney with ipsilateral ureteropelvic junction obstruction was made. We present a review of the case and of previous literature on this topic.


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Wilms' tumor in horseshoe kidney: Presen
✍ Jason G. Nirgiotis; C. Thomas Black; Joseph O. Sherman πŸ“‚ Article πŸ“… 1991 πŸ› John Wiley and Sons 🌐 English βš– 326 KB

Children with horseshoe kidney usually develop urinary tract symptoms and often require operative correction of the anomaly. The incidence of Wilms' tumor in horseshoe kidney is higher than that for the general population. We present the case of a child whose Wilms' tumor was diagnosed early because