Abstract
Rhabdomyosarcoma (RMS) represents a heterogeneous group of diseases occurring at widely diverse sites. Collectively they represent the most common soft tissue sarcomas of childhood (Young et al. 1978). Progress made in the treatment of this challenging condition has influenced pediatric oncology for 25 years and existing problems continue to challenge pediatric oncologists in all specialties. Newer molecular genetic information has been revolutionary in changing our concept of the condition.
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Cassady, J.R. (1994). Rhabdomyosarcoma. In: Cassady, J.R. (eds) Radiation Therapy in Pediatric Oncology. Medical Radiology. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-84520-8_19
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