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Cutaneous Rosai-Dorfman Disease

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DOI: 10.23977/medsc.2025.060113 | Downloads: 9 | Views: 390

Author(s)

Qian Guo 1, Xiaohua Wu 1, Chan Zhao 2

Affiliation(s)

1 First Clinical School of Medicine, Shaanxi University of Chinese Medicine, Xianyang, China
2 Department of Dermatology, Baoji Hospital of Traditional Chinese Medicine Affiliated with Shaanxi University of Chinese Medicine, Baoji, China

Corresponding Author

Qian Guo

ABSTRACT

Rosai-Dofman disease, also known as sinusoidal histiocytosis with giant lymphadenopathy, was first reported by Rosai and Dorfman in 1969. It is a rare histiocytic proliferative disease with typical .clinical features of enlarged cervical lymph nodes, fever, leukocytosis, increased sedimentation rate, anemia and hypogammaglobulinemia. Which occurs mainly in lymph nodes, and 43% of the patients have both Involvement of extranodal tissues, of which the skin is the most common site of involvement accounts for about 11%.other extranodal tissues include soft tissues, respiratory tract, genitourinary tract, oral cavity, gastrointestinal tract, orbits, testes, rarely involves the central nervous system, and only skin damage accounts for about 3%. When occurs in the skin alone and does not involve lymph nodes, it is known as cutaneous sinusoidal dyshidrotic dyshidrotic dysplasia (CRDD). CRDD usually affects middle-aged and older adults, with a female predominance, and is reported mainly in patients of Asian and Caucasian ethnicity.

KEYWORDS

Cutaneous Rosai-Dorfman Disease

CITE THIS PAPER

Qian Guo, Xiaohua Wu, Chan Zhao. Cutaneous Rosai-Dorfman Disease. MEDS Clinical Medicine (2025) Vol. 6: 86-92. DOI: http://dx.doi.org/10.23977/medsc.2025.060113.

REFERENCES

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