Literature DB >> 18627705

Langerhans cell histiocytosis: a case report and summary of the current recommendations of the Histiocyte Society.

Elizabeth K Satter1, Whitney A High.   

Abstract

Langerhans cell histiocytosis (LCH) is a rare proliferative disorder in which pathological Langerhans cells (LCs) accumulate in a variety of organs. Historically, the nomenclature regarding LCH has been confusing because the disease had been sub-categorized simply based upon different clinical manifestations. Herein, we report a child with the classic finding of disseminated LCH and summarize the current recommendation of the Histiocyte Society regarding the classification, evaluation, prognosis and treatment of LCH.

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Year:  2008        PMID: 18627705

Source DB:  PubMed          Journal:  Dermatol Online J        ISSN: 1087-2108


  2 in total

1.  Solitary congenital erosion in a newborn: report of a solitary congenital self-healing reticulohistiocytosis.

Authors:  Jung Eun Kim; Byung Jik Kim; Hoon Kang
Journal:  Ann Dermatol       Date:  2014-04-30       Impact factor: 1.444

2.  Langerhans cell histiocytosis: an illusion of hope.

Authors:  Vela D Desai; Smita R Priyadarshinni; Beena Varma; Rajeev Sharma
Journal:  Int J Clin Pediatr Dent       Date:  2013-04-26
  2 in total

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