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Primary Rosai–Dorfman disease of the femur

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Abstract

We report a 19-year-old man with the rare occurrence of primary osseous Rosai–Dorfman disease (RDD). The patient presented with a painful, solitary, bone marrow-replacing lesion in the distal femur. A diagnosis of chronic osteomyelitis was initially made on tissue from a CT-guided needle biopsy of the lesion; however, the diagnosis of RDD was eventually made after histological and immunohistochemical analysis of material from a subsequent curettage. No lymphadenopathy or other sites of involvement were found on clinical evaluation and PET-CT. To our knowledge, this is the first report of solitary osseous RDD based on systemic staging with PET-CT. We review the clinical, imaging, and histological features of primary osseous RDD, including pitfalls in diagnosis.

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Correspondence to Jonathan C. Baker.

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Baker, J.C., Kyriakos, M., McDonald, D.J. et al. Primary Rosai–Dorfman disease of the femur. Skeletal Radiol 46, 129–135 (2017). https://doi.org/10.1007/s00256-016-2515-3

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  • DOI: https://doi.org/10.1007/s00256-016-2515-3

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