Bronchiectasis is irreversible dilation of the bronchi resulting from airway damage due to a variety of causes, including infection, airway obstruction, or fibrosis.7 By definition, traction bronchiectasis results from fibrotic tissue “pulling” on the bronchi, while freestanding bronchiectasis is unrelated to fibrosis.7 Traction bronchiectasis is often seen at the periphery of the lung where there is less supportive connective tissue, leaving the bronchi prone to distortion.10 Peripheral, lower-lobe predominant traction bronchiectasis in the setting of changes consistent with fibrosis is highly suggestive of IPF.5,45

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Idiopathic Pulmonary Fibrosis (an Update) and Progressive Pulmonary Fibrosis in Adults: An Official ATS/ERS/JRS/ALAT Clinical Practice Guideline

Reference

5. Raghu G, Collard HR, Egan JJ, et al. An official ATS/ERS/JRS/ALAT statement: idiopathic pulmonary fibrosis: evidence-based guidelines for diagnosis and management. Am J Respir Crit Care Med. 2011;183:788-824.

7. Hansell DM, Bankier AA, MacMahon H, et al. Fleischner Society: glossary of terms for thoracic imaging. Radiology. 2008;246:697-722.

10. Jacob J, Hansell DM. HRCT of fibrosing lung disease. Respirology. 2015;20:859-872.

45. Raghu G, Remy-Jardin M, Myers JL, et al. Diagnosis of Idiopathic Pulmonary Fibrosis. An Official ATS/ERS/JRS/ALAT Clinical Practice Guideline. Am J Respir Crit Care Med. 2018;198(5):e44-e68.