Histiocitose de células de Langerhans: Quistos pulmonares bizarros

Authors

  • João Paulo Silva Serviço de Pneumologia, Centro Hospitalar Tondela Viseu
  • Tito Abrantes Serviço de Pneumologia, Centro Hospitalar Tondela Viseu
  • António Reis Serviço de Pneumologia, Centro Hospitalar Tondela Viseu

DOI:

https://doi.org/10.25748/arp.13817

Abstract

Langerhans cell histiocytosis (LCH) or histiocytosis X, is a rare disorder characterized by an abnormal increase in histiocyte cells, components of the immune system. Signs of LCH depend on the extent and location of the disease. A male predominance is observed.

Acta Radiológica Portuguesa

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Published

2019-01-04

Issue

Vol. 30 No. 3 (2018)

Section

Images of Interest

License

CC BY-NC 4.0