2005, Number 5
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Acta Ortop Mex 2005; 19 (5)
Sinovial sarcoma with extensive osteoid and bone formation. Case report
Albores-Zúñiga O, Domínguez-Malagón H, Cano VAM, Padilla RA, Ramírez BJ
Language: Spanish
References: 9
Page: 231-235
PDF size: 127.04 Kb.
ABSTRACT
Introduction: Sinovial Sarcoma is the fourth cause commonest of sarcomas. One appears in joints, affects minors of 40 years. A rare subtype exists, that it can accompany by formation of osteoid and bone, by immunoreactive to cytokeratin vimentin. It has prognosis and behavior more favorable than the rest of sarcomas, with survival of 80% to 5 years. Objective: To present/display a clinical case little frequents and to know the behavior neoplasia. Clinical case: Masculine of 19 years, with left shoulder tumor of 6 months of evolution, painless. The computed tomography demonstrated injury of soft parts calcified. It is put under biopsy with sinovial report of sarcoma with extensive bony formation. Intra-articular proximal humerus resection has made. Thirty months later it presents local recurrence, it was put under surgery (local resection) and it received adjuvant chemotherapy. To one year onot evidence of locoregional recurrence or metastasis. Discussion: This neoplasm is a single very rare subtype are 6 cases reported in the Literature, the prognosis and the behavior defers of the rest from sarcomas.
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