Abstract
Soft tissue sarcomas occur throughout childhood. By far the commonest is rhabdomyosarcoma, but undifferentiated embryonal sarcomas, fibrosarcomas, liposarcomas and synovial sarcomas may occur. Rhabdomyosarcoma accounts for more than 10% of childhood malignant solid tumours, and was seen in 11.3% of 612 successive children treated by the Royal Marsden Hospital and St Bartholomew’s Hospital Children’s Solid Tumour Group. It is being used as a model for development of treatment of other soft tissue sarcomas, and it will form the main subject of this chapter.
The patients presented in this report have been under the care of Dr. J. E. Freeman, Dr. J. Graham-Pole and Dr. E. R. Sandland. Dr. A. G. Stansfeld has been responsible for the histological diagnosis, and I have been much helped by Dr. J. Kingston in reviewing the data. Mr D. Hughes of the Research Centre for Mathematical Modelling of Clinical Trials at Warwick University has provided the actuarial curves. I am grateful to Jo Barton for typing the manuscript Soft Tissue Sarcomas in Children
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© 1983 Springer-Verlag Berlin · Heidelberg
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Malpas, J.S. (1983). Soft Tissue Sarcomas in Children. In: Duncan, W. (eds) Paediatric Oncology. Recent Results in Cancer Research, vol 88. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-82034-2_11
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DOI: https://doi.org/10.1007/978-3-642-82034-2_11
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