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British Journal of Radiology (2008) 81, e68-e71
© 2008 British Institute of Radiology
doi: 10.1259/bjr/53880256

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Case report

A case report of synchronous osteoblastoma and fibromatosis

H M O'DWYER, MB, BAO, BCh, FFR, RCSI 1 C F KEOGH, MB, BCh, RCSI, FRCPC 2 J X O'CONNELL, MB, BCh, FRCPC 3 and P L MUNK, MDCM, FRPC 1

1 Department of Radiology, Vancouver General Hospital, University of British Columbia, 2 Department of Radiology, British Columbia Cancer Agency, 3 Department of Pathology, Surrey Memorial Hospital, Vancouver, British Columbia, Canada

Correspondence: Professor Peter L Munk, MSK Division Head, Department of Radiology, Vancouver General Hospital, 855 West 12th Avenue, Vancouver, BC, Canada V5Z 1M9. E-mail: peter.munk{at}vch.ca

Osteoblastoma is a rare bone tumour that accounts for 1% of all primary bone tumours and 3% of all benign bone tumours. Osteoblastoma occurring in long bones has a predilection for the meta-diaphysis. It bears a close histological resemblance to osteoid osteoma, but it is not growth limited — usually 2 cm or greater at diagnosis. The term "fibromatosis" covers a broad spectrum of benign fibrous tissue proliferations. It is characterized by infiltrative growth and a tendency for recurrence; however, unlike sarcoma, it never metastasizes. To our knowledge, this is the first case report in the English literature of a patient with synchronous presentation of an osteoblastoma and fibromatosis.







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