Self‐Healing Extranodal Cutaneous Rosai‐Dorfman in a Child

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....

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Published inPediatric dermatology Vol. 32; no. 6; pp. e249 - e250
Main Authors Toledo del Castillo, Blanca, Mata‐Fernández, Cristina, Rodríguez Soria, Virna J., Parra Blanco, Verónica, Loughlin, Gerard, Campos‐Domínguez, Minia
Format Journal Article
LanguageEnglish
Published United States 01.11.2015
Subjects
Antigens, CD - metabolism
Antigens, Differentiation, Myelomonocytic - metabolism
Biomarkers - metabolism
Child, Preschool
Diagnosis, Differential
Histiocytes - metabolism
Histiocytes - pathology
Histiocytosis, Sinus - diagnosis
Histiocytosis, Sinus - metabolism
Histiocytosis, Sinus - physiopathology
Humans
Male
S100 Proteins - metabolism
Skin Diseases - diagnosis
Skin Diseases - metabolism
Skin Diseases - physiopathology
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Summary: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.
Bibliography:ObjectType-Case Study-2
SourceType-Scholarly Journals-1
ObjectType-Feature-4
content type line 23
ObjectType-Report-1
ObjectType-Article-3
ISSN:0736-8046
1525-1470
DOI:10.1111/pde.12676