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High‐grade surface osteosarcoma
Author(s) -
Staals Eric L.,
Bacchini Patrizia,
Bertoni Franco
Publication year - 2008
Publication title -
cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.052
H-Index - 304
eISSN - 1097-0142
pISSN - 0008-543X
DOI - 10.1002/cncr.23340
Subject(s) - osteosarcoma , medicine , medullary cavity , surgery , chemotherapy , retrospective cohort study , pathology
BACKGROUND High‐grade surface osteosarcoma is a rare variant of surface osteosarcoma and is associated with a poor prognosis. METHODS This retrospective study includes all cases of high‐grade surface osteosarcoma filed at the Rizzoli Institute. A complete clinical, histologic, and radiologic review was performed of 25 cases. RESULTS There were 19 males and 6 females with an average age of 21 years. All tumors were localized at the lower limb and the most frequently involved segments were the femoral and the tibial diaphysis. All lesions demonstrated the histologic aspect of a high‐grade osteosarcoma, 20 were osteoblastic, and 5 were chondroblastic. The circumferential involvement was on average 53% and in approximately half of the cases medullary canal involvement was detected. Nineteen patients underwent a combination of surgery and chemotherapy for treatment of their initial lesion, whereas 5 patients were managed with surgery alone. The average follow‐up was 9 years and the overall 5‐year survival rate was 82%. CONCLUSIONS High‐grade surface osteosarcoma is an extremely rare subtype of osteosarcoma. The current series demonstrates good overall survival for patients with this tumor. Metastatic disease and limb‐sacrificing surgery were associated with a worse prognosis. Wide surgical excision and chemotherapy might improve the outcome. Cancer 2008. ©2008 American Cancer Society.