Smoking-related idiopathic interstitial pneumonia: A review

Respirology. 2016 Jan;21(1):57-64. doi: 10.1111/resp.12576. Epub 2015 Jul 2.

Abstract

For many years, cigarette smoking has been considered as the leading cause of chronic obstructive pulmonary disease and lung cancer. Recently, however, it has also been associated with the development of diffuse interstitial lung diseases. In the latest classification of the major idiopathic interstitial pneumonias (IIP), the term smoking-related IIP has been introduced, including two entities, namely desquamative interstitial pneumonia (DIP) and respiratory bronchiolitis-interstitial lung disease (RB-ILD). Other entities in which smoking has a definite or suggested role include pulmonary Langerhan's cell histiocytosis, smoking-related interstitial fibrosis, combined pulmonary fibrosis and emphysema syndrome and idiopathic pulmonary fibrosis. In this review, we will focus on the mechanisms of smoking-related lung damage and on the clinical aspects of these disorders with the exception of idiopathic pulmonary fibrosis, which will be reviewed elsewhere in this review series.

Keywords: diagnosis; fibrosis; inflammation; nicotine; smoking; therapy.

Publication types

  • Review

MeSH terms

  • Bronchiolitis / etiology
  • Emphysema / etiology
  • Genetic Diseases, Inborn / etiology
  • Histiocytosis, Langerhans-Cell / etiology
  • Humans
  • Idiopathic Interstitial Pneumonias / etiology*
  • Lung Diseases, Interstitial / etiology
  • Pulmonary Emphysema / etiology
  • Smoking / adverse effects*

Supplementary concepts

  • Interstitial Pneumonitis, Desquamative, Familial