Ureter triplex – eine anatomische Rarität
2010
INTRODUCTION: Ureteral duplications are a common malformation of the urinary tract. A complete triplication however, is very rare. CASE REPORT: We report the case of a 26-year-old female patient admitted because of a septic disorder. Sonographic examination revealed right-sided hydronephrosis. A CT scan confirmed the rare anatomic abnormality of a ureter triplex. One of the three ureters was an obstructed mega-ureter. The dilated renal pelvis was punctured and pus drained. After clinical recovery of the patient, complete resection of the obstructed megaureter and the non-functional moiety was performed. CONCLUSION: This case illustrates an extraordinarily rare malformation of the urinary tract and describes an approach for treatment.
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