Abstract
This study highlights the clinical-paraclinical features of cystic fibrosis with multisystemic impairment in children. It is a study of 80 patients with CF, mean age 8,79±0,96 years (1 month – 38 years), and average age of cystic fibrosis diagnosis – 2,6±0,88 years. Bronchiectasis in cystic fibrosis patients was predominantly sacciforms (60 %), often with fluid levels. 25 % cystic fibrosis patients were diagnosed with pleurisy, the lung empyema was confirmed in 7,5 % of cases, pulmonary destructions – in 27,5 % cases. It was elucidated the imagistic changes in the pancreas and liver in children with cystic fibrosis.
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