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Crossed Renal Ectopia with a Fused Supernumerary Kidney
Tayeb A Rahim1, Pardeep Mittal2
1Radiology, Medical College of Georgia, Augusta University Medical Center, Augusta, USA.
Cureus
|May 19, 2020
Summary
This case report details a rare instance of coexisting renal anomalies: crossed fused renal ectopia and a supernumerary kidney. These congenital variants were unexpectedly identified in a young male presenting with flank pain and a ureteral stone.
Area of Science:
- Urology
- Congenital Anomalies
- Medical Imaging
Background:
- Crossed fused renal ectopia and supernumerary kidneys are rare congenital urinary tract anomalies.
- These conditions can be asymptomatic or associated with other developmental abnormalities.
- Early diagnosis is crucial for managing potential complications.
Observation:
- A 20-year-old male with a history of imperforate anus and tethered spinal cord presented with flank pain.
- Initial imaging suggested crossed fused renal ectopia.
- Computed tomography (CT) revealed a more complex anomaly: a supernumerary kidney fused to the right kidney, which was then fused to an orthotopic left kidney.
Findings:
- The patient had a 4-mm distal left ureteral stone.
- A supernumerary kidney was found fused to the right kidney, which was also fused to the orthotopic left kidney.
- This complex renal fusion anomaly was not detected by prior nuclear medicine renal scans or ultrasounds.
Implications:
- Highlights the importance of advanced imaging like CT in diagnosing complex congenital anomalies.
- Underscores the potential for misdiagnosis of rare renal variations with standard screening methods.
- Emphasizes the need for comprehensive evaluation in patients with multiple congenital anomalies.
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