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Autor:
Vuokko L. Kinnula, Jorma Keski-Oja, Marjukka Myllärniemi, Katri Koli, Kaisa Salmenkivi, T. Aine, Kirsi Vuorinen, Hannu Kankaanranta, Ville Pulkkinen
Publikováno v:
The Journal of Pathology. 214:456-463
Idiopathic pulmonary fibrosis (IPF) (histopathology of usual interstitial pneumonia, UIP) and non-specific interstitial pneumonia (NSIP) are diseases characterized by loss of normal lung architecture and function. The differential diagnosis between I