| Literature DB >> 26391332 |
Blanca Toledo del Castillo1, Cristina Mata-Fernández2, Virna J Rodríguez Soria3, Verónica Parra Blanco4, Gerard Loughlin1,2,3,4, Minia Campos-Domínguez3.
Abstract
Sinus histiocytosis with massive lymphadenopathy, or Rosai-Dorfman disease (RDD), is commonly characterized by painless cervical lymphadenopathy. Exclusively cutaneous Rosai-Dorfman disease is rare. In the absence of massive lymphadenopathy, the nonspecific skin lesions may complicate the diagnosis. To our knowledge, the case reported herein is the youngest case of extranodal cutaneous RDD.Entities:
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Year: 2015 PMID： 26391332 DOI： 10.1111/pde.12676
Source DB: PubMed Journal: Pediatr Dermatol ISSN： 0736-8046 Impact factor: 1.588