Bone Involvement in Rosai-Dorfman Disease (RDD): a Case Report and Systematic Literature Review
Current Rheumatology Reports, ISSN: 1534-6307, Vol: 19, Issue: 5, Page: 29
2017
- 40Citations
- 36Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations40
- Citation Indexes40
- 40
- CrossRef6
- Captures36
- Readers36
- 36
Review Description
Purpose of Review: Rosai-Dorfman disease (RDD) is a rare histiocytic disorder typically presenting as painless cervical lymphadenopathy. Extranodal involvement is common and may also affect bones. Here, we present a patient with typical nodal disease and multifocal bone manifestations. Further, a systematic literature review was performed to better understand the phenotype, clinical course and treatment options of such patients. Recent Findings: RDD is a nonmalignant, classically sporadic histiocytosis. Nevertheless, increasing evidence also suggests familial forms of the disease. According to our literature review, bone involvement is exceedingly rare and heterogeneous. Clinical outcome in terms of mortality seems to be favorable in most cases. Currently, therapy strategies include surgical and immunosuppressive treatments, but the optimal treatment of osseous RDD remains to be defined. Summary: Patients with osseous RDD may present to rheumatologists with arthralgia or arthritis. Due to the rarity of the disease, diagnosis and treatment remain challenging.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85017465868&origin=inward; http://dx.doi.org/10.1007/s11926-017-0656-6; http://www.ncbi.nlm.nih.gov/pubmed/28401384; http://link.springer.com/10.1007/s11926-017-0656-6; https://dx.doi.org/10.1007/s11926-017-0656-6; https://link.springer.com/article/10.1007/s11926-017-0656-6
Springer Science and Business Media LLC
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