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    J Bone Joint Surg Br. 2009 Sep;91(9):1223-6.

    Bone sarcomas arising in patients with neurofibromatosis type 1.

    Chowdhry M, Hughes C, Grimer RJ, Sumathi V, Wilson S, Jeys L.

    Royal Orthopaedic Hospital, Bristol Road South, Northfield, Birmingham B31 2AP, UK.

    We identified eight patients of 2900 with a primary malignant bone tumour who had coexisting neurofibromatosis type 1. This was a much higher incidence than would be expected by chance. The patients had a mean age of 22.4 years (9 to 54): five were male. Two patients subsequently developed a second bone sarcoma, one of which was radiation induced. Four of the primary tumours were osteosarcomas, four were spindle-cell sarcomas and one a Ewing's sarcoma. All the patients were treated with chemotherapy and surgery: six of the eight appear to be cured. This study suggests a possible relationship between neurofibromatosis type 1 and the development of a bone sarcoma, the increased risk being estimated at eight times that of the normal population. We recommend that further research into this possible link should be considered.

    PMID: 19721051 [PubMed - indexed for MEDLINE]

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