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Updated: Feb 28, 2026

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Establishment of Cancer Stem Cell Cultures from Human Conventional Osteosarcoma
Published on: October 14, 2016
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[Renal cell carcinomas in childhood]
L Weisbach1, A Aziz1, M Fisch1
1Klinik und Poliklinik für Urologie, Universitätsklinikum Hamburg-Eppendorf, Martinistraße 52, 20246, Hamburg, Deutschland.
Der Urologe. Ausg. A
|June 11, 2017
Summary
Childhood renal cell carcinoma (RCC) is rare, with papillary RCC being predominant. Tumor stage and lymph node status are key survival factors, necessitating interdisciplinary care and further research for advanced cases.
Area of Science:
- Pediatric Oncology
- Urologic Oncology
Background:
- Renal cell carcinoma (RCC) is a rare malignancy in children.
- It must be considered in the differential diagnosis of pediatric renal masses.
Purpose of the Study:
- To analyze the incidence, mortality, clinical presentation, diagnostics, histology, therapy, and outcomes of childhood renal cell carcinoma.
- To highlight the challenges in managing this rare pediatric cancer.
Main Methods:
- Prospective evaluation of 8 pediatric patients with renal cell carcinoma.
- Comprehensive review of current literature on pediatric RCC.
Main Results:
- Average follow-up was 27 months; no preoperative metastases were detected.
- Papillary renal cell carcinoma was the most common histological subtype.
- Tumor stage and lymph node status were identified as critical prognostic indicators.
Conclusions:
- Childhood RCC requires specialized, interdisciplinary management; typical adult symptoms are often absent.
- Partial nephrectomy is the preferred surgical approach when feasible.
- Further multicenter studies are essential to explore adjuvant therapies and understand the disease's biology and progression in advanced stages.
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