Literature DB >> 31039225

Cutaneous Rosai-Dorfman disease.

Maren Gaul1, Timothy Chang2.   

Abstract

Cutaneous Rosai-Dorfman disease (CRDD) is a rare form of Rosai-Dorfman disease (RDD)(also known as sinus histiocytosis with massive lymphadenopathy) that has a varied clinical presentation, an unknown etiology, and multiple treatment options that lack efficacy. We present a case of a 31-year-old woman who presented with grouped flesh-colored to light pink papules and plaques within a hyperpigmented patch on the thigh that were treated with topical, oral, and intralesional steroids with minimal improvement.

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Year:  2019        PMID: 31039225

Source DB:  PubMed          Journal:  Cutis        ISSN: 0011-4162


  3 in total

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

Authors:  Pan Zhang; Fang Liu; Yin Cha; Xiuying Zhang; Mei Cao
Journal:  Clin Cosmet Investig Dermatol       Date:  2021-12-24

2.  Emergence of cutaneous Rosai-Dorfman disease during immunosuppressive treatment of follicular B-cell lymphoma: A case report.

Authors:  Sharon L Kipfer; Michael Samycia; Carolyn J Shiau
Journal:  SAGE Open Med Case Rep       Date:  2021-09-16

3.  Cutaneous Rosai-Dorfman Disease: A Treatment Challenge.

Authors:  Anna Gawdzik; Bogna Ziarkiewicz-Wróblewska; Iwona Chlebicka; Alina Jankowska-Konsur; Jacek C Szepietowski; Joanna Maj
Journal:  Dermatol Ther (Heidelb)       Date:  2021-06-18
  3 in total

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