4.7 Article

Consensus recommendations for the diagnosis and clinical management of Rosai-Dorfman-Destombes disease

Journal

BLOOD
Volume 131, Issue 26, Pages 2877-2890

Publisher

AMER SOC HEMATOLOGY
DOI: 10.1182/blood-2018-03-839753

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Funding

  1. National Institutes of Health, National Cancer Institute Core Grant [P30 CA008748]
  2. American Society of Hematology Senior Research Training Award
  3. New York State Council on Graduate Medical Education Empire Clinical Research Investigator Program Fellowship from Memorial Sloan Kettering Cancer Center
  4. Frame Fund
  5. Women's Auxiliary Millennium Chair in Haematology/Oncology at The Hospital for Sick Children
  6. NATIONAL CANCER INSTITUTE [P30CA008748] Funding Source: NIH RePORTER

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Rosai-Dorfman-Destombes disease (RDD) is a rare non-Langerhans cell histiocytosis characterized by accumulation of activated histiocytes within affected tissues. RDD, which now belongs to the R group of the 2016 revised histiocytosis classification, is a widely heterogeneous entity with a range of clinical phenotypes occurring in isolation or in association with autoimmune or malignant diseases. Recent studies have found NRAS, KRAS, MAP2K1, and ARAF mutations in lesional tissues, raising the possibility of a clonal origin in some forms of RDD. More than 1000 reports have been published in the English literature; however, there is a lack of consensus regarding approach for the clinical management of RDD. Although in most cases RDD can be observed or treated with local therapies, some patients with refractory or multifocal disease experience morbidity and mortality. Here we provide the first consensus multidisciplinary recommendations for the diagnosis and management of RDD. These recommendations were discussed at the 32nd Histiocyte Society Meeting by an international group of academic clinicians and pathologists with expertise in RDD. We include guidelines for clinical, laboratory, pathologic, and radiographic evaluation of patients with RDD together with treatment recommendations based on clinical experience and review of the literature.

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