[Primary interstitial pneumopathies].

G Decroix; D Fichet; M Angebault

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PubMed · 1005268

[Primary interstitial pneumopathies].

G Decroix·D Fichet·M Angebault

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Abstract

Primitive interstitial pneumopathies are only a temporary classification. They seem to be due to an evolution for the worse of a "diffuse alveolar damage" of unknown origin. Evolution towards pulmonary fibrosis and respiratory insufficiency is their common risk. Etiopathogenic hypotheses would favour the immunological etiology. A diagnosis of primitive interstitial pneumopathy is reached by elmination when no known cause can be found. Liebow's classification remains valuable for pathology but is debatable where anatomo-clinical correlations, etiological hypotheses and the eventual effect of treatment are concerned. Today these primitive forms still represent 40% of the interstitial lung diseases, the causes of which are progressively discovered.

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G Decroix, D Fichet, M Angebault. 1976. [Primary interstitial pneumopathies].. https://pubmed.ncbi.nlm.nih.gov/1005268/

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