Non-Langerhans cell histiocytosis

From Wikipedia, the free encyclopedia
Jump to: navigation, search
Non-Langerhans cell histiocytosis
Classification and external resources
MeSH D015616

Non-Langerhans cell histiocytosis refers to a family of histiocytosis characterized by the absence of Langerhans cells.[1]

Many manifest cutaneously.[2]

the spectrum of non-langerhans cell histiocytoses include:


References[edit]

  1. ^ Weitzman S, Jaffe R (September 2005). "Uncommon histiocytic disorders: the non-Langerhans cell histiocytoses". Pediatr Blood Cancer 45 (3): 256–64. doi:10.1002/pbc.20246. PMID 15547923. 
  2. ^ Philip T. Cagle; Timothy C. Allen; Roberto Barrios (1 December 2007). Color atlas and text of pulmonary pathology. Lippincott Williams & Wilkins. pp. 210–. ISBN 978-0-7817-8208-1. Retrieved 14 November 2010. 
  3. ^ Rao RN, Chang CC, Uysal N, Presberg K, Shidham VB, Tomashefski JF (February 2005). "Fulminant multisystem non-langerhans cell histiocytic proliferation with hemophagocytosis: a variant form of Erdheim-Chester disease". Arch. Pathol. Lab. Med. 129 (2): e39–43. doi:10.1043/1543-2165(2005)129<e39:FMNCHP>2.0.CO;2. PMID 15679446.