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Published in: Clinical Orthopaedics and Related Research® 7/2009

01-07-2009 | Original Article

Infarct-associated Bone Sarcomas

Authors: Gregory F. Domson, MD, Amir Shahlaee, MD, John D. Reith, MD, Charles H. Bush, MD, C. Parker Gibbs, MD

Published in: Clinical Orthopaedics and Related Research® | Issue 7/2009

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Abstract

Sarcoma associated with bone infarct is a rare condition sparsely reported in the literature. Sixty percent of cases arise about the knee and most are malignant fibrous histiocytomas. We report 15 patients; 12 of 15 presented with a tumor around the knee. Treatment was limb salvage in seven patients, amputation in six, and biopsy alone in two. For patients without metastatic disease at presentation, the 2-year disease-free survival rate was 63% (seven of 11). Two patients received chemotherapy and both were continuously disease-free at last followup. When we combined our 15 patients with the 52 previously reported in the literature, 38 of the 67 (57%) died of their disease at an average of 19.2 months after diagnosis; 21 patients (31%) were continuously disease-free for 24 months. Of 13 patients who received chemotherapy, eight (62%) were continuously disease-free at 24 months compared with 24% (13 of 54) of those who did not receive chemotherapy. Overall, prognosis for these patients is poor, but survival in patients without metastatic disease at diagnosis approaches that of other bone sarcomas. There is a trend suggesting adjuvant chemotherapy combined with appropriate surgery may improve patient outcomes.
Level of Evidence: Level IV, therapeutic study. See the Guidelines for Authors for a complete description of levels of evidence.
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Metadata
Title
Infarct-associated Bone Sarcomas
Authors
Gregory F. Domson, MD
Amir Shahlaee, MD
John D. Reith, MD
Charles H. Bush, MD
C. Parker Gibbs, MD
Publication date
01-07-2009
Publisher
Springer-Verlag
Published in
Clinical Orthopaedics and Related Research® / Issue 7/2009
Print ISSN: 0009-921X
Electronic ISSN: 1528-1132
DOI
https://doi.org/10.1007/s11999-009-0744-7

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