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. 2015 Dec 8;47(4):446-50.
doi: 10.1016/S2255-4971(15)30126-9. eCollection 2012 Jul-Aug.

EWING'S SARCOMA: EPIDEMIOLOGY AND PROGNOSIS FOR PATIENTS TREATED AT THE PEDIATRIC ONCOLOGY INSTITUTE, IOP-GRAACC-UNIFESP

Affiliations

EWING'S SARCOMA: EPIDEMIOLOGY AND PROGNOSIS FOR PATIENTS TREATED AT THE PEDIATRIC ONCOLOGY INSTITUTE, IOP-GRAACC-UNIFESP

Davi Gabriel Bellan et al. Rev Bras Ortop. .

Abstract

Objective: To outline the epidemiological profile and prognosis for Ewing's sarcoma in the Brazilian population.

Material and methods: The medical records of 64 patients with intraosseous Ewing's sarcoma who were treated at the Pediatric Oncology Institute, IOP-GRAACC-Unifesp, between 1995 and 2010, were retrospectively evaluated.

Results: The statistical analysis on the data obtained did not correlate factors such as sex, trauma, pathological fracture and time taken for case diagnosis with the treatment outcome. Factors such as initial metastasis, lung metastasis, tumor site, age, recurrence and type of surgery showed results corroborating what has been established in the literature.

Conclusion: The prognosis in cases of Ewing's sarcoma was mainly influenced by the presence of metastases at the time of diagnosis.

Keywords: Bone Neoplasms; Prognosis; Sarcoma, Ewing.

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Figures

Figure 1
Figure 1
Ten-year-old patient with pain in the proximal region of the left humerus for three months: (A) radiograph showing mixed lesion (osteolytic and osteoblastic), with periosteal reactions in “sunray” pattern and presence of Codman triangle; (B) magnetic resonance imaging showing lesion in the proximal third of the humerus, invading the epiphysis, and also an extraosseous mass; (C) radiograph after resection of the lesion and reconstruction using vascularized fibular tissue, while preserving the fibular proximal epiphysis to enable growth.
Figure 2
Figure 2
Survival of the patients treated due to Ewing's tumor.

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