| Literature DB >> 27785544 |
Jonathan C Baker1, Michael Kyriakos2, Douglas J McDonald3, David A Rubin4.
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.Entities:
Keywords: Bone biopsy; Rosai–Dorfman disease; Sinus histiocytosis with massive lymphadenopathy
Mesh:
Year: 2016 PMID: 27785544 DOI: 10.1007/s00256-016-2515-3
Source DB: PubMed Journal: Skeletal Radiol ISSN: 0364-2348 Impact factor: 2.199