A Rare and unique case of Bilateral Double Collecting System with Congenital Ureteric anomalies presenting as abdominal distension in  a two–year old baby girl

Md. Aasif Siddique Ahmed Khan; Sukanya Muddusetty; A. Narendra Kumar; Kavitha N.; Bushra Raoof; Shashank Kumar Srivastav.

Volume : IV, Issue : VII, July - 2015

A Rare and unique case of Bilateral Double Collecting System with Congenital Ureteric anomalies presenting as abdominal distension in a two–year old baby girl

Md. Aasif Siddique Ahmed Khan, Sukanya Muddusetty, A. Narendra Kumar, Kavitha N. , Bushra Raoof, Shashank Kumar Srivastav.

Abstract :

 Development disorders of kidneys and urinary tract constitute a spectrum of malformations ranging from the complete absence of kidney tissue to minor structural abnormalities. We report a unique case of malrotated duplex kidney with complete duplication of ureter with upper moiety grossly dilated tortuous ureter suggestive of Congenital Giant Megaureter (CGM) on Right side and duplex kidney on left side with partial duplication of ureter in a two year old female child which presented as abdominal distension since birth. Such anomaly with the normal function and drainage in both the kidneys has not been reported so far, in this age group.