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Updated: May 24, 2026

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Murine Bilateral Renal Lymphadenectomy
Published on: December 30, 2025
Bilateral renal cell carcinoma in a child
Jonathan Cloutier1, Anis Aziz, Brant Inman
1Division of Urology, Centre Hospitalier Universitaire de Québec (CHUQ), Université Laval, Quebec, Canada.
Urology
|March 6, 2012
Summary
This study details the first reported case of bilateral renal clear cell carcinoma in a child, successfully treated with partial nephrectomies. Long-term follow-up showed no recurrence and preserved normal kidney function.
Area of Science:
- Pediatric Oncology
- Nephrology
- Genetics
Background:
- Renal cell carcinoma (RCC) is a rare malignancy in children, accounting for 0.1-0.3% of pediatric tumors.
- Clear cell RCC is the most common histologic subtype of adult RCC but is exceptionally rare in pediatric cases.
Observation:
- This report presents the first documented case of bilateral renal clear cell carcinoma in a pediatric patient.
- The patient underwent bilateral partial nephrectomies for tumor removal.
Findings:
- Comprehensive genetic evaluation was performed to rule out hereditary cancer syndromes.
- Analysis focused on chromosomal deletions associated with renal cell carcinoma subtypes.
- The patient experienced no tumor recurrence during an 80-month follow-up period.
- Post-treatment renal function remained within normal limits.
Implications:
- This case highlights the possibility of bilateral clear cell RCC in pediatric patients, even without a family history.
- Successful management with partial nephrectomies preserves renal function, offering a potential therapeutic approach.
- Further research into the genetic underpinnings of pediatric clear cell RCC is warranted.
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