Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2022 Jul 26;15(1):263.
doi: 10.1186/s13104-022-06156-3.

Morphological features of bronchiectasis in patients with non-tuberculous mycobacteriosis and interstitial pneumonia

Affiliations

Morphological features of bronchiectasis in patients with non-tuberculous mycobacteriosis and interstitial pneumonia

Chiori Tabe et al. BMC Res Notes. .

Abstract

Objective: To compare the morphological features of bronchiectasis between patients with different underlying diseases, we performed quantitative analysis of high-resolution computed tomography (HRCT) images of 14 patients with non-tuberculous mycobacteriosis (NTM) and 13 with idiopathic pulmonary fibrosis (IPF). A 3D image of the bronchial structure was made from HRCT data. Bronchiectasis was defined as abnormal dilatation of the bronchi with the diameter greater than that of the accompanying pulmonary artery. We measured the inner and outer diameters, wall area as %total airway cross sectional area (WA%), and wall thickness to airway diameter ratio (T/D) of the 4-8th generations of bronchi.

Results: In patients with IPF, the inner and outer diameters linearly decreased toward the distal bronchi. In contrast, the inner and outer diameters of NTM fluctuated. The coefficient of variation of the outer diameters of the 6-7th generations of bronchi was larger in the NTM patients than in those with IPF, whereas no significant difference was observed in the coefficient of variation of the inner diameters between the groups. In IPF patients, WA% and T/D varied between the generation of bronchi, but the coefficient of variation of WA% and T/D was relatively small in those with NTM.

Keywords: 3D image; Bronchial structure; Bronchiectasis; Idiopathic pulmonary fibrosis; Non-tuberculous mycobacteriosis.

PubMed Disclaimer

Conflict of interest statement

The authors declare that they have no competing interests.

Figures

Fig. 1
Fig. 1
Measurement procedure using a CT-3D imaging workstation. The bronchus to be measured was selected on the left CT image, and a bronchial pathway was created by automatic extraction (top). The bronchial cross section at the specified position is displayed and the inner and outer diameters are marked (bottom left). The inner and outer diameters, WA%, and T/D ratio were automatically calculated for the 4th-8th generations of bronchi (bottom right). L: lumen diameter, T: wall thickness, D: overall bronchial diameter. In the measurement screen, multiple measurements of T, D, and L are made, and their average are calculated
Fig. 2
Fig. 2
Morphological parameters of bronchiectasis. A Outer diameter, B Inner diameter. In the patients with IPF, the outer and inner diameters decreased linearly toward the distal part of the bronchus. In contrast, some bronchi were larger at the distal part, and the outer and inner diameter measurements of a generation of the bronchi were largely different between the patients with NTM. C WA%, D T/D ratio. WA% and T/D ratio in most of the NTM patients increased linearly toward the distal part of the bronchus although the values were diverse between the subjects. In the patients with IPF, larger values of WA% and T/D ratio were observed at the distal part
Fig. 3
Fig. 3
Schematic diagram of morphological features of bronchiectasis. Bronchiectasis in NTM patients has a larger lumen and thicker walls due to edematous changes of the bronchial wall, whereas IPF patients have a larger lumen and thinner airway wall due to traction along with the fibrosis of the surrounding alveoli

References

    1. McShane PJ, Tino G. Bronchiectasis. Chest. 2019;155:825–833. doi: 10.1016/j.chest.2018.10.027. - DOI - PubMed
    1. Martinez-Garcia MA, Polverino E, Aksamit T. Bronchiectasis and chronic airway disease: it is not just about asthma and COPD. Chest. 2018;154:737–739. doi: 10.1016/j.chest.2018.02.024. - DOI - PubMed
    1. Izhakian S, Wasser WG, Fuks L, Vainshelboim B, Fox BD, Fruchter O, Kramer MR. Lobar distribution in non-cystic fibrosis bronchiectasis predicts bacteriologic pathogen treatment. Eur J Clin Microbiol Infect Dis. 2016;35:791–796. doi: 10.1007/s10096-016-2599-7. - DOI - PubMed
    1. McShane PJ, Naureckas ET, Tino G, Strek ME. Non-cystic fibrosis bronchiectasis. Am J Respir Crit Care Med. 2013;188:647–656. doi: 10.1164/rccm.201303-0411CI. - DOI - PubMed
    1. Kadowaki T, Yano S, Wakabayashi K, Kobayashi K, Ishikawa S, Kimura M, Ikeda T. An analysis of etiology, causal pathogens, imaging patterns, and treatment of Japanese patients with bronchiectasis. Respir Investing. 2015;53:37–44. doi: 10.1016/j.resinv.2014.09.004. - DOI - PubMed

MeSH terms

LinkOut - more resources