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  3. Vol. 2 No. 2 (2014): Spring
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Spring
Vol. 2 No. 2 (2014)

Giant Hydronephrosis Due to Congenital Uretropelvic Junction Obstruction, a Report of 2 cases

  • Simin Sadeghi-Bojd
  • Faramarz Fazeli
  • kambiz keshavarz
  • Maryam Baktash

Journal of Pediatric Nephrology, Vol. 2 No. 2 (2014), , Page 83-86
https://doi.org/10.22037/jpn.v2i2.5658 Published 17 April 2014

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Abstract

Ureteropelvic junction (UPJ) stenosis occurs in 13% of children. Antenatally, the diagnosis is possible by showing renal pelvis dilatation by obstetric ultrasonography. Giant hydronephrosis (GH) is a rare condition. There are different etiologies for GH which are mostly congenital and occur during infancy and childhood. GH was confirmed by complementary evaluations in a 2-month-old female infant with poor feeding, lethargy, and vomiting together with an antenatal sonography in favor of hydronephrosis, and a 5-year-old boy with an abdominal mass diagnosed by sonography following 2 weeks of progressive abdominal distention. Pyeloplasty was associated with an excellent result in both of them.

Keywords: Hydronephrosis; Ureteral Obstruction; Congenital; Urologic Diseases.

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How to Cite

1.
Sadeghi-Bojd S, Fazeli F, keshavarz kambiz, Baktash M. Giant Hydronephrosis Due to Congenital Uretropelvic Junction Obstruction, a Report of 2 cases. J Ped Nephrol [Internet]. 2014Apr.17 [cited 2022Jun.30];2(2):83-6. Available from: https://journals.sbmu.ac.ir/jpn/article/view/5658
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