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Approach to Incidental Findings in the Lung

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What we can do when approaching lung cancer screening

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cts is both use our eyes visually,

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but we can also quantify some of the findings.

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We can visually assess emphysema, how severe is it

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and where is it distributed In the lungs.

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We can look at small airway while thickening

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and categorize it as mild, moderate, severe, depending on

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how small the airway lumen has become relative

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to the thickness of the wall.

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We can look for mucus plugging

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and even a few scattered small mucus plugs is now known

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to be associated with increased patient morbidity

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and poor outcomes and bronchiectasis With emphysema,

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we can not only apply this visual rating of non mild,

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moderate, severe, but there are many tools now

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that will quantify emphysema

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and make that easy to put in your radiology reports as well

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as to follow the severity over time.

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And then there's interstitial lung abnormalities

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and fibrotic disease.

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ILA or interstitial lung abnormalities are incidentally

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detected and represent early evidence of pulmonary fibrosis.

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When we see these, whether it's on a lung cancer screening,

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CT or any chest ct, we should recommend referral

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to pulmonary medicine with pulmonary function testing,

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as well as testing for connective tissue disease,

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which most pulmonary medicine physicians will undertake

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because of the increased association with ILAs.

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When patients are asymptomatic

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and have normal functions with no evidence of CTD

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patients should be followed up with pulmonary medicine

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and usually do so annually with pulmonary function tests

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or if they develop symptoms

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because abnormality in pulmonary function tests developing

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or new symptoms is indicative

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of pulmonary fibrosis progression

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for which antifibrotic therapies may then become indicated.

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We know that 10 to 20% of patients with this mild evidence

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of interstitial lung disease found on

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chest cts incidentally, including our lung cancer screening,

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cts, will progress over the next five to 10 years.

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Here's an example of a 61-year-old baseline CT has mild

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peripheral subpleural reticulation

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and is asymptomatic at this time with normal pft,

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but nine months later becomes symptomatic.

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CT is repeated and we can see

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that the disease extent has already progressed in the short

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term at this time.

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Through both of these time points.

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Serologic tests remain negative with no evidence

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of connective tissue disease.

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This serial CT examination is the same patient

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taken from the position paper from the Fleischer Society on

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interstitial lung abnormalities,

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which is a really good reference for this topic

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and reviews the literature quite well.

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This study is out of the COPD gene study,

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which is a longitudinal study of COPD,

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looking at ways to identify it earlier, understand it,

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and to treat it so that we can prevent progression.

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This patient in A-C-O-P-D study, which is A-C-O-P-D study,

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not a fibrotic lung disease study, starts out

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with a baseline CT with just some mild subtle reticulation

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that might even go referred to as a little bit

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of dependent ectasis

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because there's not much else that was seen

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four years later on their COPD gene research study.

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We now see areas of dilated bronchi in the lung periphery

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and more reticulation.

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By 2010, we now see convincing evidence,

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much more extensive amount of ground glass reticulation,

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traction bronchiectasis,

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and then through 2015,

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12 years since the original detection,

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we have considerable progression yet again

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and starting to develop small honeycomb cysts.

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So ILAs at their earliest when we identify them.

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Patients with these findings should be referred

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for pulmonary medicine function testing

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and pulmonary consultation

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to both understand the disease at current state

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and decide whether antifibrotic therapies are important

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today or should be used in the future if disease progresses

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or symptoms are identified.

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And lastly, I wanna talk briefly about quantitative analysis

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of cts using tools

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that can help us extract information from cts.

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They can be applied both to interstitial lung disease,

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looking for areas of increased lung density, ground glass,

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and reticulation and subcategorize, those findings as well

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as applied to emphysema to quantify the severity

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of emphysema or to quantify small airway disease

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by measuring the amount of air trapping.

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This is an example of looking at interstitial lung disease

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using one of these quantitative tools

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where we can look at the normal lung shown in green,

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whether it's superimposed on a coronal image,

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whether it's using these sort of radar diagrams.

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So you can see each lobe

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and the extent of each different feature.

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In this patient. We have ground glass demarcated.

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In this yellow color, we have reticular in the orange color

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and we had no honeycombing.

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So we can measure how much disease is present versus

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how much normal lung,

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and we can measure the type of underlying abnormality.

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Ground glass, generally more reversible.

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Honeycombing and reticulation, generally irreversible.

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If we're using antifibrotic medications, we can look

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to see if they're having impact on the rate

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of progression is slowing or the disease is held in check.

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And we can break these findings down into details

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to each lung, each lobe, and so on.

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Most of these tools were originally developed

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through radiologist ground truthing

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of individual little vox.

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And I participated in a number of these studies

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where we took small pieces of the lung, as you can see here,

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little voxel groupings of the lung

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and decided whether they were ground glass, reticular,

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honeycombing, normal lung,

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and so on, so the tools could be developed to identify them.

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And so most of the tools out there today have used some form

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of radiologist ground truthing

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as their underpinning in the way they quantify lung disease.

Report

Faculty

Ella A. Kazerooni, MD, MS

Professor of Radiology, Cardiothoracic Division

University of Michigan

Tags

Oncologic Imaging

Lungs

Chest

Acquired/Developmental