Abstract
Childhood tumours are rare in our environment, lymphomas, nephroblastoma and leukemias may be found but embryonal rhabdomyosarcoma (botryoid sarcoma) is not only rare but is the most lethal. A case of a 3-year old girl (see photographs 1 & 11) who was referred to UCTH with a recurrent vaginal mass is presented. Histology of the biopsy specimen confirmed embryonal rhabdomyosarcoma. Delay in referring this case to a Tertiary center by health workers, late presentation with advanced disease, poor financial status of the parents and high cost of treatment all contributed to the mortality in this unfortunate child. Mary Slessor Journal of Medicine Vol.3(2) 2003: 30-31
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