## Abstract ## Background A retrospective analysis of the results and relapse pattern was evaluated in 34 patients with Ewing's family bone tumors (EFBT) treated at Rizzoli Institute with neoadjuvant chemotherapy between 1983 and 2003. ## Objectives The aim of the study was to evaluate treatment
Ewing's sarcoma of the ribs
โ Scribed by P.R.M. Thomas; M. Tefft; R.G. Evans; M.E. Nesbit
- Publisher
- Elsevier Science
- Year
- 1981
- Tongue
- English
- Weight
- 171 KB
- Volume
- 7
- Category
- Article
- ISSN
- 0360-3016
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
Between 1984Between -1987, 50 , 50 patients with Ewing's sarcoma of the bone were entered on combined modality protocol at Tata Memorial Hospital. Protocol treatment involved induction therapy consisting of 6-week therapy with vincristine, Adriamycin (doxorubicin), and cyclophosphamide (VDC) follow
par irradiation (6/31 = 19,4%). La maladie a OtO un peu mieux contr610e localement chez les patients traitOs par la chirurgie: 27,3% de rOcidives locales au lieu de 38, 7% chez les malades irradiOs seulement. Cette diffOrence n'est cependant pas statistiquement significative. Les rOsultats de cette
## Background: Ewing's sarcoma usually is identified as a primary malignancy of bone affecting children and young adults. extraskeletal ewing's sarcoma is rare, and very few data are available addressing optimal surgical and oncologic treatment modalities. ## Methods: The authors chose to review
## Abstract A rare case of Ewing's sarcoma of the toe bone is described and compared with three reported cases of phalangeal Ewing's sarcoma. The lesion in two cases was initially treated as infection and the diagnosis was delayed for several months. Roentgenographic and aspiration cytology examina