High-resolution computed tomography in the diagnosis and follow-up of idiopathic pulmonary fibrosis View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2010-01-15

AUTHORS

N. Sverzellati, M. De Filippo, T. Bartalena, S. Piciucchi, M. Zompatori

ABSTRACT

Idiopathic pulmonary fibrosis (IPF) is the most common interstitial lung disease and is associated with a fatal prognosis. Familiarity with the typical appearances of IPF on high-resolution computed tomography (HRCT) is important, as in the appropriate clinical setting, it is often sufficient for establishing a confident diagnosis of IPF without the need for surgical biopsy. Moreover, HRCT can provide important prognostic information in IPF. This is noteworthy, as the course of IPF is variable, and many patients develop complications leading to respiratory failure and death. The purpose of this paper is to review the progress made towards a better understanding of the HRCT patterns of IPF. More... »

PAGES

526-538

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s11547-010-0512-5

DOI

http://dx.doi.org/10.1007/s11547-010-0512-5

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1050301361

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/20082223


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