| Literature DB >> 18631399 |
Holger Gerullis1, Christoph Eimer, Dietmar Betz, Thomas Otto.
Abstract
INTRODUCTION: Horseshoe kidney is a rare congenital malformation that is found in approximately 0.25% of the general population and usually remains asymptomatic. CASEEntities:
Year: 2008 PMID: 18631399 PMCID: PMC2488349 DOI: 10.1186/1752-1947-2-231
Source DB: PubMed Journal: J Med Case Rep ISSN: 1752-1947
Figure 1Preoperative situation. The atrophic right moiety of the horseshoe kidney with uretero-pelvic junction obstruction, consecutive hydronephrosis and normal distal right ureter are shown. The left moiety showing hydronephrosis due to a relative stricture of uretero-pelvic junction in combination with two distal ureteral strictures can also be seen (in situ ureteral stent not shown).
Figure 2Intraoperative situation. Heminephrectomy of the right moiety with dissection of the right ureter, excision of the uretero-pelvic stricture followed by transposition of the right ureter to the left pelvis (transureteropyelostomy).
Figure 3Postoperative situation with improvement of urine drainage of the left pelvis via two ureters. Residual hydronephrosis was regressive after 2 months.