Primary tibial bone involvement in Rosai Dorfman Disease treated with surgery and radiotherapy; case report and literature review

Rosai-Dorfman disease is a rare benign disease that is characterized by over-production and accumulation of white blood cells, known as (histiocytes) in the lymph nodes (nodal) or any other areas of the body (extranodal). It usually presents as painless, massive cervical lymphadenopathy. Extranodal disease involvement is also common but isolated primary involvement of bone is rare. We present a case of isolated primary tibial bone involvement in Rosai-Dorfman disease as the only presentation. It was treated with surgery in the form of curettage and bone cementing with adjuvant radiotherapy. Five years of follow-up did not show any recurrence or disease dissemination.

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Journal
Journal of Orthopaedic Reports
Published
2025-03-04
DOI
https://doi.org/10.1016/j.jorep.2025.100612
Citations
1
Primary Topic
Histiocytic Disorders and Treatments
Type
article
Field-Weighted Citation Impact
1.16
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article

Primary tibial bone involvement in Rosai Dorfman Disease treated with surgery and radiotherapy; case report and literature review

Hassan Sawan, Talal Alrawaf, Osama Alshaya, Abdullah Alotibi et al.
1 citations
Journal of Orthopaedic Reports
Histiocytic Disorders and Treatments
1.16
article

Primary tibial bone involvement in Rosai Dorfman Disease treated with surgery and radiotherapy; case report and literature review

Hassan Sawan, Talal Alrawaf, Osama Alshaya, Abdullah Alotibi, Muath Aljufayr
article en
1 citations

Abstract

Rosai-Dorfman disease is a rare benign disease that is characterized by over-production and accumulation of white blood cells, known as (histiocytes) in the lymph nodes (nodal) or any other areas of the body (extranodal). It usually presents as painless, massive cervical lymphadenopathy. Extranodal disease involvement is also common but isolated primary involvement of bone is rare. We present a case of isolated primary tibial bone involvement in Rosai-Dorfman disease as the only presentation. It was treated with surgery in the form of curettage and bone cementing with adjuvant radiotherapy. Five years of follow-up did not show any recurrence or disease dissemination.

Journal of Orthopaedic ReportsVol. 4(2)
King Fahd Medical City (SA)
Good health and well-being
Openalex Percentile: Top 25%
Histiocytic Disorders and Treatments
1.16
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