0000000000660707

AUTHOR

M. Wiebel

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Pulmonary emphysema in cystic fibrosis detected by densitometry on chest multidetector computed tomography.

2013

BackgroundHistopathological studies on lung specimens from patients with cystic fibrosis (CF) and recent results from a mouse model indicate that emphysema may contribute to CF lung disease. However, little is known about the relevance of emphysema in patients with CF. In the present study, we used computationally generated density masks based on multidetector computed tomography (MDCT) of the chest for non-invasive characterization and quantification of emphysema in CF.MethodsVolumetric MDCT scans were acquired in parallel to pulmonary function testing in 41 patients with CF (median age 20.1 years; range 7-66 years) and 21 non-CF controls (median age 30.4 years; range 4-68 years), and subj…

AdultMalemedicine.medical_specialtyAdolescentCystic FibrosisScienceCystic fibrosisPulmonary function testingHounsfield scaleMultidetector computed tomographyMedicineHumansLung volumesChildAgedEmphysemaMultidisciplinaryLungbusiness.industryQCase-control studyRMiddle Agedrespiratory systemmedicine.diseaserespiratory tract diseasesmedicine.anatomical_structureCase-Control StudiesMedicineFemaleRadiologybusinessDensitometryTomography X-Ray ComputedResearch ArticlePLoS ONE
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