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A preexisting condition was found in 9\/47 (19%) patients including neurofibromatosis (3), Down's syndrome (1), spina bifida (1), congenital facial asymmetry (1), giant pigmented nevus (1), juvenile onset diabetes mellitus (1), and acquired immune deficiency syndrome (1). The site of primary tumor was head and neck (3), trunk (33), and extremities (11). Twenty\u2010four patients (51%) have survived free of disease with a median follow\u2010up of 5 years (4 months\u201022 years). No patient whose disease recurred achieved a second remission. Of the 19 patients with group I disease, 16 (84%) survived free of disease. Wide excision of the primary tumor, with no microscopic residual disease, was associated with the greatest chance of disease\u2010freesurvival.<\/jats:p>","DOI":"10.1002\/mpo.2950200205","type":"journal-article","created":{"date-parts":[[2007,2,20]],"date-time":"2007-02-20T18:21:47Z","timestamp":1171995707000},"page":"114-118","source":"Crossref","is-referenced-by-count":19,"title":["Soft\u2010tissue sarcomas other than rhabdomyosarcoma in children"],"prefix":"10.1002","volume":"20","author":[{"given":"Ammar","family":"Hayani","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"suffix":"Jr.","given":"Donald H.","family":"Mahoney","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hal K.","family":"Hawkins","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"C. 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