-
Comparative Study
Radiologic computed tomography features of Mycobacterium abscessus in cystic fibrosis.
- Diana L Lam, Siddhartha G Kapnadak, J David Godwin, Gregory A Kicska, Moira L Aitken, and Sudhakar N Pipavath.
- Department of Radiology, University of Washington School of Medicine, Seattle, WA, 98195, USA.
- Clin Respir J. 2018 Feb 1; 12 (2): 459-466.
IntroductionMycobacterium abscessus infection in cystic fibrosis (CF) patients can lead to poor outcomes. Early diagnosis is important, but there are no studies outlining specific imaging features of M. abscessus in CF.ObjectivesTo describe the computed tomography (CT) findings of early M. abscessus infection in our CF population.MethodsThirteen CF patients with sputum cultures positive for M. abscessus from 2006 to 2013 were identified at our institution. Clinical characteristics including culture dates and lung function were reviewed. Positive cultures were classified as "disease" versus "colonization" based on published criteria. Chest CT scans were reviewed at times closest to initial infection, and features including bronchiectasis, mucous plugging, consolidation, ground glass opacities, nodules, and cavitation were evaluated. Brody scores were calculated to evaluate extent of CF lung disease.ResultsAll patients had bronchiectasis and mucous plugging, with 10 of 13 (76.9%) in an upper lobe distribution. Consolidation was seen in 12 of 13 (92.3%) patients, 8 (61.5%) patients had nodules, and 5 (38.5%) with cavitation. The average Brody score was 59.5, which was no different than previously described CF cohorts without M. abscessus. There were no significant differences between subjects with disease versus colonization.ConclusionThe most common CT features of early M. abscessus in our CF population include bronchiectasis, mucus plugging, and consolidation, but the findings did not reveal a unique radiologic signature. CT at this initial time point may not distinguish early M. abscessus infection from background lung disease or mycobacterial colonization in CF patients.© 2016 John Wiley & Sons Ltd.
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