High-Resolution Computed Tomography of Fibrotic Interstitial Lung Disease

被引:5
|
作者
Rodriguez, Karen [1 ]
Ashby, Christian L. [2 ]
Varela, Valeria R. [2 ]
Sharma, Amita [1 ]
机构
[1] Massachusetts Gen Hosp, Dept Radiol, Div Thorac Imaging & Intervent, Austen 202,55 Fruit St, Boston, MA 02114 USA
[2] Univ Cent Caribe, Sch Med, Bayamon, PR USA
关键词
interstitial lung disease; high-resolution computed tomography; fibrosis; traction bronchiectasis; honeycombing; fibrotic sarcoidosis; IDIOPATHIC PULMONARY-FIBROSIS; CHRONIC HYPERSENSITIVITY PNEUMONITIS; THIN-SECTION CT; RESPIRATORY-DISTRESS-SYNDROME; PLEUROPARENCHYMAL FIBROELASTOSIS; TRACTION BRONCHIECTASIS; CLINICAL PREDICTORS; DIAGNOSTIC-CRITERIA; FLEISCHNER-SOCIETY; FUNCTION INDEXES;
D O I
10.1055/s-0042-1755563
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
While radiography is the first-line imaging technique for evaluation of pulmonary disease, high-resolution computed tomography (HRCT) provides detailed assessment of the lung parenchyma and interstitium, allowing normal anatomy to be differentiated from superimposed abnormal findings. The fibrotic interstitial lung diseases have HRCT features that include reticulation, traction bronchiectasis and bronchiolectasis, honeycombing, architectural distortion, and volume loss. The characterization and distribution of these features result in distinctive CT patterns. The CT pattern and its progression over time can be combined with clinical, serologic, and pathologic data during multidisciplinary discussion to establish a clinical diagnosis. Serial examinations identify progression, treatment response, complications, and can assist in determining prognosis. This article will describe the technique used to perform HRCT, the normal and abnormal appearance of the lung on HRCT, and the CT patterns identified in common fibrotic lung diseases.
引用
收藏
页码:764 / 779
页数:16
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