Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
3824019 | Progrès en Urologie | 2010 | 5 Pages |
Abstract
A stenosis of the upper pole of an incomplete renal duplication is presented. The prenatal diagnosis of a right renal ureteropyelic junction syndrome, isolated, with a normal amniotic liquid was confirmed at birth. Intravenous pyelogram 8Â days after birth showed three right dilated calical groups with a dilated renal ureteropyelic junction, but an normal inferior calical group suspected a renal bifidity. Renal MagIII scintigraphy evaluated the anatomical and functional stenosis and indicated surgery. Postoperative followings were simple and results good 3Â years after. From this rare case, embryogenesis is discussed.
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Authors
D.M. Bourdelat, C. Mazzola,