SciELO - Scientific Electronic Library Online

 
vol.19 issue1Follow up relevance in the secondary prevention of ischemic heart disease with atorvastatin: Pilot studyAcute adrenal insuficiency caused by adrenal hemorrhage as a first manifestation of the antiphospholipid syndrome: A case report and review author indexsubject indexarticles search
Home Pagealphabetic serial listing  

Services on Demand

Journal

Article

Indicators

Related links

  • On index processCited by Google
  • Have no similar articlesSimilars in SciELO
  • On index processSimilars in Google

Share


Anales de Medicina Interna

Print version ISSN 0212-7199

Abstract

ABELLAN MARTINEZ, Mª. C. et al. Pulmonary histiocytosis X: A case report and literature review. An. Med. Interna (Madrid) [online]. 2002, vol.19, n.1, pp.16-18. ISSN 0212-7199.

Histiocytosis X or Langerhans cell histiocytosis is an unfrequent disease, which consists on proliferation of Langerhans cells. The etiology is unknown. Diagnosis is reached by electron microscope study of the biopsy, in which the Birbeck intracitoplasmatic granules of the Langerhans cells are found and/or by inmunohistochemistry procedures able to detect S-100 antigen and CD1 cells. Diagnosis can also be reached with a bronchoalveolar lavage in which CD1 cells will appear in a score higher than 5%.  We present the case of a 16 year-old girl that first appeared with a pulmonar lesion with a honey comb X-ray pattern and unsintomatic mandibular bone affectation. Diagnosis was reached by biopsy study using S-100 antigen detection procedures. We consider this case an important one due to the unfrequency of this particular disease. 

Keywords : Histiocytosis; Langerhans cells; Eosinophilic granuloma.

        · abstract in Spanish     · text in Spanish     · Spanish ( pdf )

 

Creative Commons License All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License