Comprehensive Quantification of Lung Structure and Function

6-27-01

Figure 1: This montage depicts a stack of CT sections (lower left); a three-dimensional airway tree (center); a tumor obstructing the bronchial tree, incl. the tumor's association with surrounding major vascular structures (upper and lower right); a bronchoscopic image of the obstructed airway tree (left-center); and a superposed graph showing objective measures of airway cross-sectional area as a function of distance down the tree. Such imaging is currently being used on a regular basis for custom-designed interventions to eliminate obstructions via laser surgery and/or to build custom stents to hold open the obstructed segment. Quantitative methods are now allowing for the accurate measurement of airway segments as small as 1 mm in diameter, with sub-millimeter accuracy.
 
 
 

 

Figure 2: To image pulmonary blood flow, iodinated contrast agent is injected into the blood stream at the right side of the heart. Rapid CT scanning, gated to the heartbeat during a breath hold, allows for the reconstruction of the regional brightness changes that occur throughout the lung in response to the passage of the injected agent. Left panel: three-dimensional images of the lungs and a three-dimensional heart (opened digitally by the computer). Center: a cross-sectional image of the lungs shows regions of interest from which time-intensity curves have been measured. Upper right: by comparing these curves with the time-intensity curve sampled from within the area of the pulmonary artery, it is now possible to calculate the timing of a red blood cell through the microvascular beds of the lung. Disruption of flow parameters at the microvascular level is believed to provide the earliest sign of the onset of inflammatory lung disease leading to, for instance, emphysema and fibrosis.
 
 
 
 
 
 
 
Figure 3: Non-radioactive xenon gas is radio-dense and serves as a tag of regional
ventilation. A patient re-breathes a fixed percentage of xenon gas (40% or less) and
images are obtained through multi-slice spiral CT scanning at the same point of
each expiratory pause. The brightness change in the reconstructed CT image
provides information about the rate of wash-in/wash-out of the xenon gas and thus
regional ventilation. Upper left: a subject in a CT scanner attached to a computer
system, which monitors lung volume and controls the delivery of xenon gas. Upper
right: brightness change as xenon gas is washed out of the lung. Lower left: a
color-coded image that quantitatively represents brightness changes due to xenon
gas. Center: volumetric images of the lung scanned at two points within the
respiratory cycle.
 
 
 
 
 
 
 
Figure 4: Methods are emerging that allow the computer to use mathematical formulations of "texture." These methods describe the patterns of bright and dark regions in the CT images to discriminate between tissue types and to provide a report of the amount and distribution of pathologic processes. Upper part: a method identifying the portion of the lung that falls below a particular gray scale range, defining it as being emphysema-like. Such a method is useful in identifying mild to severe emphysema without other co-existing patterns of disease. Using a more advanced form of tissue characterization (lower part), the computer can evaluate the image based upon 50 or more mathematical formulations of the patterns of gray scale variations. It color-codes the CT slice according to tissue patterns, such as emphysema-like, ground glass, broncho-vascular, nodular, honeycomb, etc.

 

 
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