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Autosomal recessive multisystem disorder caused by dysfunctional chloride ion transport across epithelial surfaces → thickening of secretions (e.g., mucus, digestive fluids, sweat)
In lungs, abnormal mucus & degraded WBCs → chronic airway impaction → recurrent inflammation & infections → chronic airway damage (in progressively worsening cycle)
Most common in upper lobes, superior lower lobes
Peribronchial thickening (early finding)
Mosaic attenuation due to air-trapping, best seen on expiratory CT
Bronchiectasis with signet ring sign (bronchus larger than adjacent artery)
Mucus plugging within dilated bronchi (finger-in-glove appearance)
Tree-in-bud centrilobular nodular opacities on CT
Most common lethal genetic disorder in Caucasians
∼ 1 in 2,500 affected
Mutation in both copies of CF transmembrane conductance regulator ( CFTR ) gene at chromosome 7q31.2 → defective chloride transport → abnormal water regulation
> 1,000 genetic defects can result in CF; ΔF508 mutation of CFTR most common (∼ 90%)
70% present < 1 year of age: GI symptoms more common
90% by 12 years of age: Respiratory more typical
Often have asthma-type symptoms
Median survival: 41.1 years
Annual chest radiograph or low-dose surveillance CT
CT best assesses progressive disease & predicts future exacerbations vs. pulmonary function tests, radiographs
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