Duplex collecting system with renal malrotation: an unusual combination

Authors

  • Raden H. P. S. Secodiningrat Department of Urology, Primaya Hospital PGI Cikini, Jakarta, Indonesia
  • Nicholas A. Singgih Department of Urology, Primaya Hospital PGI Cikini, Jakarta, Indonesia
  • Jacinda R. Oktaviani Department of Urology, Primaya Hospital PGI Cikini, Jakarta, Indonesia
  • Egi E. Manuputty Department of Urology, Primaya Hospital PGI Cikini, Jakarta, Indonesia

DOI:

https://doi.org/10.18203/2349-2902.isj20231739

Keywords:

Bifid renal pelvis, Duplex kidney, Malrotation kidney, Renal fusion anomaly, Reverse rotation kidney

Abstract

Both duplex collecting system and renal malrotation are congenital developmental anomalies of kidney. They usually present asymptomatic and accidentally diagnosed while patients undergo radiology examinations. We are reporting a case of a 33-year-old-male with a combination of duplex and malrotation kidney. Although these two are common anomalies of kidney, their combination is extremely rare. We found only two reports that had similar combined cases, so our case is the third reported.

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References

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Published

2023-05-30

Issue

Section

Case Reports