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Acta Radiol ; 47(8): 798-800, 2006 Oct.
Article in English | MEDLINE | ID: mdl-17050358

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.


Subject(s)
Bronchi/abnormalities , Bronchiectasis/diagnostic imaging , Cartilage/abnormalities , Tomography, Spiral Computed , Bronchiectasis/congenital , Bronchiectasis/etiology , Humans , Syndrome
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