| Literature DB >> 17050358 |
V Di Scioscio1, M Zompatori, I Mistura, P Montanari, L Santilli, R Luccaroni, N Sverzellati.
Abstract
Williams-Campbell syndrome is a cystic bronchiectatic disease secondary to deficiency or defect of cartilaginous plates in the wall of the airways. In the literature, two main forms are suggested: congenital and acquired (post-infectious). The most frequent symptoms are represented by recurrent pulmonary infections from childhood. Multislice spiral dynamic CT has a major role in the study of cystic pulmonary disease and in differentiating Williams-Campbell syndrome from the other causes of cystic bronchiectasis, in which even lung function tests can give deceptive results.Entities:
Mesh:
Year: 2006 PMID: 17050358 DOI: 10.1080/02841850600849084
Source DB: PubMed Journal: Acta Radiol ISSN: 0284-1851 Impact factor: 1.990