Published on
​Pathology - Bronchiectasis
An irreversible enlargement of many airways, transmural bronchial inflammation or infection, and persistent mucopurulent sputum production are the hallmarks of bronchiectasis. Bronchiectasis is a common pathologic finding in CF. This condition is often classified into two classes: that which is caused by CF and that which is not CF related. Instead of having cystic fibrosis (CF), the patient in the vignette has chronic lung disease (COPD), which involves long-term inflammation that eventually damages the airways and causes cilia malfunction. The damage that results increases the lung's susceptibility to recurring infections, which are frequently observed in this illness. The same factors that make patients with pulmonary tuberculosis (TB) more prone to bronchiectasis also make them more vulnerable to inflammation and persistent lung infections. The cause of clubbing of the digits is unknown, yet it is observed in certain chronic pulmonary diseases (lung cancer, severe TB, and CF). To maintain lung function in these patients, aggressive secretion control and prompt infection detection are critical.
Picture
0 Comments