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Benign cephalic histiocytosis with diabetes insipidus.
Weston, W L; Travers, S H; Mierau, G W; Heasley, D; Fitzpatrick, J.
Afiliación
  • Weston WL; Departments of Dermatology and Pediatrics, University of Colorado School of Medicine, and Department of Pathology, Children's Hospital, Denver, Denver, Colorado, USA. william.weston@exchange.UCHSC.edu
Pediatr Dermatol ; 17(4): 296-8, 2000.
Article en En | MEDLINE | ID: mdl-10990580
Benign cephalic histiocytosis is a rare skin condition consisting of small tan papules on the face and upper trunk that is believed not to be associated with internal organ involvement. The infiltrating histiocytes are not Langerhans' cells (LCs). We report a 5-year-old girl who presented with diabetes insipidus 1 year after developing multiple small brown asymptomatic skin papules. Histologic examination revealed a non-LC histiocytic proliferation in the dermis without epidermal invasion. She had infiltration of the pituitary stalk on brain imaging. Diabetes insipidus has heretofore been associated with LC histiocytosis and xanthoma disseminatum but not benign cephalic histiocytosis.
Asunto(s)
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedades de la Piel / Histiocitosis de Células no Langerhans / Diabetes Insípida Límite: Child, preschool / Female / Humans Idioma: En Revista: Pediatr Dermatol Año: 2000 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedades de la Piel / Histiocitosis de Células no Langerhans / Diabetes Insípida Límite: Child, preschool / Female / Humans Idioma: En Revista: Pediatr Dermatol Año: 2000 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos