Journal of Clinical Medicine (Aug 2019)

Pulmonary Fibrosis in Children

  • Nadia Nathan,
  • Chiara Sileo,
  • Guillaume Thouvenin,
  • Laura Berdah,
  • Céline Delestrain,
  • Effrosyne Manali,
  • Spyros Papiris,
  • Pierre-Louis Léger,
  • Hubert Ducou le Pointe,
  • Aurore Coulomb l’Hermine,
  • Annick Clement

DOI
https://doi.org/10.3390/jcm8091312
Journal volume & issue
Vol. 8, no. 9
p. 1312

Abstract

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Pulmonary fibrosis (PF) is a very rare condition in children, which may be observed in specific forms of interstitial lung disease. None of the clinical, radiological, or histological descriptions used for PF diagnosis in adult patients, especially in situations of idiopathic PF, can apply to pediatric situations. This observation supports the view that PF expression may differ with age and, most likely, may cover distinct entities. The present review aims at summarizing the current understanding of PF pathophysiology in children and identifying suitable diagnostic criteria.

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