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Research ArticleOriginal Article
Open Access

Renal cell carcinoma in children. Prognostic factors

Mohammad O. Al-Shabanah, Derek R. Jenkin, Yasser O. Khafaga, Ali M. Al-Zahrani, Cyril Danjoux and Mark Greenberg
Saudi Medical Journal November 2004, 25 (11) 1583-1586;
Mohammad O. Al-Shabanah
Section of Radiation Oncology, MBC-64, King Faisal Specialist Hospital and Research Centre, PO Box 3354, Riyadh 11211, Kingdom of Saudi Arabia. Tel. +966 (1) 4423940. Fax. +966 (1) 4424566. E-mail: [email protected]
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Derek R. Jenkin
Section of Radiation Oncology, Department of Oncology, King Faisal Specialist Hospital and Research Centre, Riyadh, Kingdom of Saudi Arabia
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Yasser O. Khafaga
Section of Radiation Oncology, Department of Oncology, King Faisal Specialist Hospital and Research Centre, Riyadh, Kingdom of Saudi Arabia
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Ali M. Al-Zahrani
Section of Radiation Oncology, Department of Oncology, King Faisal Specialist Hospital and Research Centre, Riyadh, Kingdom of Saudi Arabia
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Cyril Danjoux
Division of Radiation Oncology, Toronto-Sunnybrook Regional Cancer Centre, North York, Toronto, Canada
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Mark Greenberg
Division of Pediatric Hematology/Oncology, Department of Pediatrics, The Hospital For Sick Children, Toronto, Canada.
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Abstract

OBJECTIVE: To determine the outcome in childhood renal cell carcinoma and the role of surgical and radiation treatment.

METHODS: The records of 21 children with renal cell carcinoma were reviewed, 15 patients treated in the University of Toronto centers from 1959 through to 1997 and 6 patients treated in King Faisal Specialist Hospital, Riyadh, Kingdom of Saudi Arabia from 1975 through to 1998. The age was 3-17 (median 13) years. Systematic metastases were present at diagnosis in 5 patients. Regional nodal spread was present in 9 patients and 7 patients had localized disease alone. In the 16 M0 patients, the surgical treatment was radical nephrectomy (14 patients) partial nephrectomy (one patient) and wedge resection (one patient). Postoperative radiation treatment was utilized in 8 (50%) of these patients.

RESULTS: The 5 year survival rate for all patients was 52%, and for M0 patients was 70%. No patient with systematic metastases at diagnosis survived beyond 26 months. Four of 7 node negative patients and 8 of 9 node positive patients remained in first complete remission, with the duration of follow up 1-30 (Median 5) years. Seven of 8 M0 patients who did not receive adjuvant radiation therapy continued in first remission (3N0, 2NI, 2N2), compared with 5 of 8 patients who received postoperativeradiation treatment (1 N0, 2 NI, 2 N2).

CONCLUSION: The prognosis of localized renal cell carcinoma in childhood may be better than in the adult. Gross complete resection is required for long term survival. Elective postoperativeradiation treatment is not indicated.

  • Copyright: © Saudi Medical Journal

This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Saudi Medical Journal: 25 (11)
Saudi Medical Journal
Vol. 25, Issue 11
1 Nov 2004
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Renal cell carcinoma in children. Prognostic factors
Mohammad O. Al-Shabanah, Derek R. Jenkin, Yasser O. Khafaga, Ali M. Al-Zahrani, Cyril Danjoux, Mark Greenberg
Saudi Medical Journal Nov 2004, 25 (11) 1583-1586;

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Renal cell carcinoma in children. Prognostic factors
Mohammad O. Al-Shabanah, Derek R. Jenkin, Yasser O. Khafaga, Ali M. Al-Zahrani, Cyril Danjoux, Mark Greenberg
Saudi Medical Journal Nov 2004, 25 (11) 1583-1586;
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© 2025 Saudi Medical Journal Saudi Medical Journal is copyright under the Berne Convention and the International Copyright Convention.  Saudi Medical Journal is an Open Access journal and articles published are distributed under the terms of the Creative Commons Attribution-NonCommercial License (CC BY-NC). Readers may copy, distribute, and display the work for non-commercial purposes with the proper citation of the original work. Electronic ISSN 1658-3175. Print ISSN 0379-5284.

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