JOURNAL ARTICLE

[Idiopathic interstitial pneumonia: classification and diagnostic work-up]

Thierry Rochat, Jean-Claude Pache
Revue Médicale Suisse 2010 November 24, 6 (272): 2222-7
21207733
Idiopathic interstitial pneumonias represent a group of complex lung diseases among which the most frequent types are idiopathic pulmonary fibrosis (IPF), idiopathic non-specific interstitial pneumonia (idiopathic NSIP), and cryptogenic organizing pneumonia (COP). Clinicians may rely on a precise classification of these diseases from an America-European consensus that has been published in 2002. However it appears that diagnosis should always be confirmed by a multidisciplinary team discussion with experience in the field. There are generally tremendous prognostic and therapeutic implications for the patient.

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