Volume 60, Issue 4 pp. 250-256
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Ewing's sarcoma of bone: Oncologic and functional results

Auke J. S. Renard MD

Auke J. S. Renard MD

Departments of Orthopaedics, University of Nijmegen, Nijmegen, The Netherlands

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Dr. René P. H. Veth MD, PhD

Corresponding Author

Dr. René P. H. Veth MD, PhD

Departments of Orthopaedics, University of Nijmegen, Nijmegen, The Netherlands

Department of Orthopaedics, University Hospital of St. Radboud, University of Nijmegen, P.O. Box 9101, NL-6500 HB, Nijmegen, The NetherlandsSearch for more papers by this author
Maciej Pruszczynksi MD, PhD

Maciej Pruszczynksi MD, PhD

Departments of Pathology, University of Nijmegen, Nijmegen, The Netherlands

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Jaap Hoogenhout MD, PhD

Jaap Hoogenhout MD, PhD

Departments of Radiotherapy, University of Nijmegen, Nijmegen, The Netherlands

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Jos Bökkerink MD, PhD

Jos Bökkerink MD, PhD

Departments of Pediatric Oncology, University of Nijmegen, Nijmegen, The Netherlands

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Frans J. M. Van Der Staak

Frans J. M. Van Der Staak

Departments of Pediatric Surgery, University of Nijmegen, Nijmegen, The Netherlands

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Theo Wobbes MD, PhD

Theo Wobbes MD, PhD

Departments of General Surgery, University of Nijmegen, Nijmegen, The Netherlands

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Josef A. M. Lemmens MD, PhD

Josef A. M. Lemmens MD, PhD

Departments of Radiology, University of Nijmegen, Nijmegen, The Netherlands

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René van Hoesel MD, PhD

René van Hoesel MD, PhD

Departments of Medical Oncology, University Hospital of St. Radboud, University of Nijmegen, Nijmegen, The Netherlands

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Jim R. Van Horn MD, PhD

Jim R. Van Horn MD, PhD

Department of Orthopaedics, University Hospital of Croningen, Groningen, The Netherlands

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First published: December 1995
Citations: 9

Abstract

This paper describes 29 patients with Ewing's sarcoma of bone treated between 1975 and 1990 at the University of Nijmegen Hospital, Nijmegen, The Netherlands. Osteomyelitis was the primary diagnosis in 24%.

Treatment consisted of chemotherapy in combination with surgery and/or radiotherapy. Nine patients received radiotherapy only; five of them died of disease. Five patients underwent an intralesional excision; four of them died of disease. Twelve patients underwent a wide excision; there is no evidence of disease in any of them. Three patients underwent a radical disarticulation; all died of disease. The disease-free survival at 1.5 years was 66%. This figure at 5 years was 55%. After wide excision and reconstruction in tumors of expendable, femoral or radial bones good functional results were obtained in all cases. © 1995 Wiley-Liss, Inc.

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