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Cutaneous Rosai-Dorfman disease is a rare, lymphoproliferative disease. It is benign and self-limited, only involves skin and subcutaneous tissue and typically occurs as histiocyte-rich inflammatory infiltrates, manifesting as erythematous to brown papules, plaques, or nodules, without predilection...

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Bibliographic Details
Main Authors: Han Ma (Author), Huaiqiu Huang (Author), Meirong Li (Author), Wei Lai (Author), Chun Lu (Author)
Format: Book
Published: Sociedade Brasileira de Dermatologia, 2014-01-01T00:00:00Z.
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Summary:Cutaneous Rosai-Dorfman disease is a rare, lymphoproliferative disease. It is benign and self-limited, only involves skin and subcutaneous tissue and typically occurs as histiocyte-rich inflammatory infiltrates, manifesting as erythematous to brown papules, plaques, or nodules, without predilection for site. The authors describe a case of cutaneous Rosai-Dorfman disease in a 72-year-old man who presented erythematous and scaled plaque on the right neck for three months without systemic symptoms. Owing to local involvement, the patient received a surgery to exsect the lesion completely and remained asymptomatic with no signs of recurrence at the 9-month follow up.
Item Description:0365-0596
10.1590/abd1806-4841.20142485