Literature DB >> 8075000

Histiocytosis--an introduction.

J Pritchard1, V Broadbent.   

Abstract

The Histiocytoses are a group of rare and puzzling multisystem disorders, currently regarded as non-malignant but often treated with 'cancer chemotherapy'. In this article, the origins of histiocytes and of the Histiocyte Society's classification of the Histiocytoses are described with suggested minor modifications to the classification. The current nomenclature for the 2 principal diseases, now named 'Langerhans cell histiocytosis' and 'Haemophagocytic Lymphohistiocytosis', is less confusing than the terms originally chosen. The article sets the scene for the succeeding papers, which focus on 'Langerhans cell histiocytosis'.

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Mesh:

Year:  1994        PMID: 8075000      PMCID: PMC2149703     

Source DB:  PubMed          Journal:  Br J Cancer Suppl        ISSN: 0306-9443


  2 in total

1.  Histiocytosis X; integration of eosinophilic granuloma of bone, Letterer-Siwe disease, and Schüller-Christian disease as related manifestations of a single nosologic entity.

Authors:  L LICHTENSTEIN
Journal:  AMA Arch Pathol       Date:  1953-07

Review 2.  Histiocytosis X histogenetic arguments for a Langerhans cell origin.

Authors:  C Nezelof; F Basset; M F Rousseau
Journal:  Biomedicine       Date:  1973-09
  2 in total
  5 in total

1.  Endocrine aspects of Langerhans cell histiocytosis.

Authors:  A T Soliman; I Alsalmi; N E Banna; M Asfour
Journal:  Indian J Pediatr       Date:  1996 May-Jun       Impact factor: 1.967

Review 2.  Langerhans cell histiocytosis (histiocytosis X).

Authors:  K Y Lam
Journal:  Postgrad Med J       Date:  1997-07       Impact factor: 2.401

3.  An unusual cause of limp.

Authors:  Mehdi Garbash; Vidhooshni Rajamoorthy; Shrinavas Tambe; John Schofield; Nikila Pandya
Journal:  BMJ Case Rep       Date:  2012-04-04

4.  Mutations in SLC29A3, encoding an equilibrative nucleoside transporter ENT3, cause a familial histiocytosis syndrome (Faisalabad histiocytosis) and familial Rosai-Dorfman disease.

Authors:  Neil V Morgan; Mark R Morris; Hakan Cangul; Diane Gleeson; Anna Straatman-Iwanowska; Nicholas Davies; Stephen Keenan; Shanaz Pasha; Fatimah Rahman; Dean Gentle; Maaike P G Vreeswijk; Peter Devilee; Margaret A Knowles; Serdar Ceylaner; Richard C Trembath; Carlos Dalence; Erol Kismet; Vedat Köseoğlu; Hans-Christoph Rossbach; Paul Gissen; David Tannahill; Eamonn R Maher
Journal:  PLoS Genet       Date:  2010-02-05       Impact factor: 5.917

5.  Multisystem Langerhans cell histiocytosis presenting as an oral lesion.

Authors:  Kallarakkal Thomas George; Ramanathan Anand; Sockalingam Ganasalingam; Rosnah B Zain
Journal:  J Oral Maxillofac Pathol       Date:  2013-01
  5 in total

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