Today, many people with the disease live into their 40s and 50s, and even longer in some cases.
The histological pattern of UIP Fig. In some cases, both lungs may need to be replaced. Sinusitis is almost universal, and nasal polyposis is frequently present.
Sweat Chloride Test The sweat chloride test is the most commonly used test for diagnosing cystic fibrosis. Ancillary features of cystic fibrosis may be of diagnostic assistance eg, nasal polyposis, Pseudomonas aeruginosa in sputum, azoospermia, and others.
Nonsteroidal anti-inflammatory drugs NSAIDssuch as ibuprofen and indomethacin, may help reduce any pain and fever associated with cystic fibrosis.
CT Scan A CT scan creates detailed images of the body by using a combination of X-rays taken from many different directions. Get influenza and pneumonia vaccinations regularly. Biopsies should be obtained in more than one lobe, and if possible, the middle lobe and lingula should be avoided, as they usually show non-specific changes that do not provide diagnostic information.