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Case Report

Self-Limited Primary Cutaneous Rosai-Dorfman Disease: A Case Report and Literature Review

, ORCID Icon, , & ORCID Icon
Pages 1879-1884 | Published online: 24 Dec 2021

References

  • Gawdzik A, Ziarkiewicz-Wróblewska B, Chlebicka I, Jankowska-Konsur A, Szepietowski JC, Maj J. Cutaneous Rosai–Dorfman disease: a treatment challenge. Dermatol Ther. 2021;11(4):1443–1448. doi:10.1007/s13555-021-00557-1
  • Rosai J, Dorfman RF. Sinus histiocytosis with massive lymphadenopathy. A newly recognized benign clinicopathological entity. Arch Pathol. 1969;87(1):63–70.
  • Emile JF, Abla O, Fraitag S, et al. Revised classification of histiocytoses and neoplasms of the macrophage-dendritic cell lineages. Blood. 2016;127(22):2672–2681. PMID: 26966089; PMCID: PMC5161007. doi:10.1182/blood-2016-01-690636
  • Bruce-Brand C, Schneider JW, Schubert P. Rosai–Dorfman disease: an overview. J Clin Pathol. 2020;73(11):697–705. doi:10.1136/jclinpath-2020-206733
  • Fayne R, Rengifo SS, Gonzalez I, et al. Primary cutaneous Rosai–Dorfman disease; a case-based review of a diagnostically and therapeutically challenging rare variant. Ann Diagn Pathol. 2020;45:151446. doi:10.1016/j.anndiagpath.2019.151446
  • Zhang Y, Chen H, Jiang YQ, et al. Clinicopathological features of cutaneous Rosai–Dorfman disease and its relationship to IgG4-related disease: a retrospective study. Br J Dermatol. 2019;181(4):844–845. doi:10.1111/bjd.17939
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