Abstract
Isolation of mucoid strains of Pseudomonas aeruginosa from bronchial secretions has occurred usually in the setting of cystic fibrosis. This association has been so strong that it is considered a sign of the presence of cystic fibrosis. We reviewed the records of 31 patients in whom this strain was isolated; in contract to previous experiences, we found that only 2 of our patients could be considered to have cystic fibrosis. The remainder all had a chronic pulmonary disease, and common to all was the presence of bronchiectasis. We conclude that isolation of mucoid strains of Pseudomonas aeruginosa from bronchial secretions of adults with a chronic pulmonary process indicates the presence of underlying bronchiectasis.
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