A case of cutaneous Rosai-Dorfman disease (CRDD) with underlying calvarial involvement and absence of BRAFV600E mutation

Kaskas, Nadine M.; Kern, Malan; Johnson, Andrew P.; Hughes, Matthew; Hardee, Matthew E.; Day, John D.; Gökden, Murat; Shalin, Sara C.; Gao, Ling

doi:10.1016/j.jdcr.2015.10.003

Cited by 6 publications

(3 citation statements)

References 15 publications

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“…However, the patient developed a lesion in his spine and agreed to undergo additional surgical treatment. One case similar to our patient was reported during the past few years, and doctors opted for surgical resection ( 11 ). There is still no consensus regarding the best clinical treatment for CRDD, but different methods have been reported for many types of CRDD, such as cryotherapy, radiotherapy, steroid injections, or treatment with systemic corticosteroids, retinoids, dapsone, imatinib mesylate, or thalidomide, which is recommended in the NCCN guidelines ( 12 – 15 ).…”

Section: Discussionsupporting

confidence: 74%

A primary Rosai-Dorfman-Destombes disease of the scalp: case report and literature review

et al. 2023

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BackgroundRosai-Dorfman-Destombes disease (RDD) was first described in 1965 as a benign histiocytic proliferative disorder of unknown cause. Cases of RDD limited to cutaneous tissue have been reported over the past few decades, but single cutaneous RDD of the scalp is rare.Case presentationWe report a 31-year-old male with a lump on the parietal scalp without extranodal lesion lasting 1 month with gradual enlargement. The surgical incision ruptured with purulent after the first resection. Then the patient was treated with plastic surgery after disinfection and antibiotic treatment. Finally, he recovered well and discharged after 20 days.ConclusionsRDD of the scalp is rare. Surgical incision can cure the lesion but it may become infected because of increased lymphocytic infiltration. Early diagnosis and differential diagnosis of RDD are necessary. For treatment, individualized therapy is critical to patient prognosis.

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Section: Discussionsupporting

confidence: 74%

A primary Rosai-Dorfman-Destombes disease of the scalp: case report and literature review

et al. 2023

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“…The histologic characteristics of RDD include an inflammatory infiltrate with numerous plasma cells and histiocytes, which have a large pale eosinophilic cytoplasm, vesicular nuclei, and positive staining for S-100 and CD68, but negative staining for CD1a. 9 …”

Section: Discussionmentioning

confidence: 99%

Multifocal Rosai-Dorfman disease with involvement of the pinna

Hirt

Heskett²,

Veerula³

et al. 2017

JAAD Case Reports

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“…Five cases of CRDD of the scalp have been reported (4 primary skull RDD with subcutaneous infiltration and 1 primary CRDD of the scalp) [1]. Accumulation of RDD on PET/CT has been reported [2].…”

Section: Discussionmentioning

confidence: 99%