These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Search MEDLINE/PubMed


  • Title: Langerhans cell histiocytosis: a review of the current recommendations of the Histiocyte Society.
    Author: Satter EK, High WA.
    Journal: Pediatr Dermatol; 2008; 25(3):291-5. PubMed ID: 18577030.
    Abstract:
    Langerhans cell histiocytosis is a rare proliferative disorder where pathologic Langerhans cells accumulate in a variety of organs. Historically, the nomenclature regarding this entity has been confusing because the disease had been subcategorized simply based upon the different clinical manifestations. In the following article, we summarize the current recommendation of the Histiocyte Society regarding the classification, evaluation, prognosis, and treatment of Langerhans cell histiocytosis.
    [Abstract] [Full Text] [Related] [New Search]