{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,11,3]],"date-time":"2026-11-03T17:23:17Z","timestamp":1793726597722,"version":"4.6.1"},"reference-count":169,"publisher":"Georg Thieme Verlag KG","issue":"06","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Semin Respir Crit Care Med"],"published-print":{"date-parts":[[2022,12]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:p>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.<\/jats:p>","DOI":"10.1055\/s-0042-1755563","type":"journal-article","created":{"date-parts":[[2022,10,28]],"date-time":"2022-10-28T20:06:16Z","timestamp":1666987576000},"page":"764-779","source":"Crossref","is-referenced-by-count":14,"title":["High-Resolution Computed Tomography of Fibrotic Interstitial Lung Disease"],"prefix":"10.1055","volume":"43","author":[{"given":"Karen","family":"Rodriguez","sequence":"additional","affiliation":[{"name":"Division of Thoracic Imaging and Intervention, Department of Radiology, Massachusetts General Hospital, Boston, Massachusetts"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Christian L.","family":"Ashby","sequence":"additional","affiliation":[{"name":"School of Medicine, Universidad Central del Caribe School of Medicine, Bayam\u00f3n, Puerto Rico"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Valeria R.","family":"Varela","sequence":"additional","affiliation":[{"name":"School of Medicine, Universidad Central del Caribe School of Medicine, Bayam\u00f3n, Puerto Rico"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Amita","family":"Sharma","sequence":"additional","affiliation":[{"name":"Division of Thoracic Imaging and Intervention, Department of Radiology, Massachusetts General Hospital, Boston, Massachusetts"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"194","published-online":{"date-parts":[[2022,10,28]]},"reference":[{"issue":"02","key":"ref1","doi-asserted-by":"crossref","first-page":"138","DOI":"10.1016\/S2213-2600(17)30433-2","article-title":"Diagnostic criteria for idiopathic pulmonary fibrosis: a Fleischner Society White Paper","volume":"6","author":"D A Lynch","year":"2018","journal-title":"Lancet Respir Med"},{"issue":"02","key":"ref2","doi-asserted-by":"crossref","first-page":"141","DOI":"10.1164\/rccm.201208-1544CI","article-title":"Fibrosing interstitial lung disease. 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