• Revue médicale suisse · Nov 2010

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

    • Thierry Rochat and Jean-Claude Pache.
    • Service de pneumologie, HUG, 1211 Genève 14. thierry.rochat@hcuge.ch
    • Rev Med Suisse. 2010 Nov 24; 6 (272): 2222-7.

    AbstractIdiopathic 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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