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SMALL AIRWAY DISEASES - 09/09/11

Doi : 10.1016/S0033-8389(05)70012-9 
Sylvia A. Worthy, MRCP, FRCR a, Nestor L. Müller, MD, PhD b
a Department of Radiology, Royal Victoria Infirmary, Newcastle upon Tyne (SAW), United Kingdom 
b Department of Radiology, Vancouver Hospital and Health Sciences Centre and University of British Columbia, Vancouver, British Columbia (NLM), Canada 

Riassunto

The term small airways is generally used to refer to airways 3 mm or less in diameter, the vast majority of which represent bronchioles.19 Bronchioles are divided into membranous bronchioles that function purely as an air-conducting system and respiratory bronchioles that contain alveoli within their walls and are thus involved in respiration. Bronchioles measure approximately 0.5 to 1 mm in diameter. The small airways contribute very little to resistance because, being so numerous, their overall cross-sectional area is large. Consequently, there may be considerable destruction of the small airways before the patient becomes symptomatic and there is any detectable abnormality of pulmonary function.19 Abnormalities of the small airways may originate within these airways themselves or result from extension of diseases involving either the larger bronchi or the lung parenchyma.19

In order to appreciate the high-resolution CT (HRCT) scan changes found in small airway diseases it is necessary to have an understanding of the anatomy of the normal secondary pulmonary lobule. The secondary pulmonary lobule is defined as the smallest portion of lung surrounded by connective tissue septa.19 It measures 10 to 25 mm in diameter. The bronchiole and branch of the pulmonary artery supplying the secondary pulmonary lobule are located in its center, whereas branches of the pulmonary veins are located peripherally within the interlobular septa. The lobular bronchiole divides into three or more terminal membranous bronchioles that each divide into respiratory bronchioles that then branch into alveolar ducts. Thus, the bronchioles are centrilobular structures being clustered near the center of a secondary pulmonary lobule. This accounts for the characteristic centrilobular distribution of bronchiolar abnormalities on HRCT scan. The bronchioles within a secondary pulmonary lobule measure less than 1 mm in diameter11 and have a wall thickness of less than 0.1 mm. This is below the limit of visibility on HRCT scan and thus normal centrilobular bronchioles are too small to be visualized.20 Normally, the only centrilobular structure to be identified on HRCT scan is the pulmonary artery branch. Any additional centrilobular opacities are abnormal.

HRCT scan is currently the best imaging technique for assessment of diseases of the bronchioles.9 Window settings influence the apparent size of structures, particularly small ones, such as bronchioles.15 Measurement of airway diameter is most accurate at a window level of −450 H28; however, this is not generally used in clinical practice because it gives suboptimal demonstration of the lung parenchyma. A window level of −700 H and a window width of 1000 to 1500 H is recommended for optimal depiction of the airways and lung parenchyma. It should be appreciated, however, that this results in an underestimation of true bronchial diameter.16

There is no universally accepted single protocol for assessing small airways disease.19 We recommend and use a combination of 1-mm collimation scans at 10-mm intervals through the lungs at end-inspiration and end-expiration scans at five equally spaced levels from the top of the aortic arch to just above the right hemidiaphragm.19 The end-expiratory scans are essential for the detection of air-trapping.

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 Address reprint requests to Nestor L. Müller, MD, PhD, Department of Radiology, Vancouver Hospital and Health Sciences Centre, 855 West 12th Avenue, Vancouver, BC, Canada V5Z 1M9


© 1998  W. B. Saunders Company. Pubblicato da Elsevier Masson SAS. Tutti i diritti riservati.
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Vol 36 - N° 1

P. 163-173 - gennaio 1998 Ritorno al numero
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