High-Resolution CT of the Lung Textbook: A Clinical Reference Covering Interstitial, Airway, and Vascular Disease Patterns for Thoracic Radiology Fellows - Softcover

Houle MD, Anthony S.

9798190852059: High-Resolution CT of the Lung Textbook: A Clinical Reference Covering Interstitial, Airway, and Vascular Disease Patterns for Thoracic Radiology Fellows

Softcover

ISBN 13: 9798190852059

Publisher: Independently published, 2026

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Built for the reader who must turn a gray-scale volume into a confidence-graded diagnosis before the multidisciplinary team convenes, this reference grounds every HRCT read in the anatomy of the secondary pulmonary lobule, then carries that foundation through a fixed distribution-pattern-ancillary-findings algorithm into a four-tier confidence framework that states, in one honest word, how far a single study can carry a diagnosis alone. It moves from the fibrotic differential that decides biopsy and antifibrotic eligibility, through the nodular, cystic, and airway-centered patterns that define sarcoidosis, LAM, and small airways disease, into the acute and special-population contexts where the same discipline must hold under real technical constraint. It serves the thoracic radiology fellow, the resident on chest call, and the pulmonologist reading alongside radiology.

Confidence-tiered pattern callouts, cross-referenced cases, and a consolidated point-of-care atlas turn a compressed differential into a defensible report.

Inside, You Will Learn How To

• Grade the UIP call — apply the typical, probable, indeterminate, and alternative-diagnosis tiers that decide whether idiopathic pulmonary fibrosis needs biopsy.

• Separate NSIP from UIP — read subpleural sparing and symmetry against the finding whose absence caps a pattern below typical.

• Read exposure into the image — apply multilobar air trapping and the head-cheese sign to redirect fibrosis toward hypersensitivity pneumonitis.

• Stage sarcoidosis and defend it — correlate perilymphatic nodularity and centrilobular sparing against carcinomatosis, silicosis, and infection.

• Name the cyst — distinguish LAM, Birt-Hogg-Dub� syndrome, and lymphocytic interstitial pneumonia by shape, distribution, and wall.

• Confirm the mosaic — apply expiratory accentuation to separate airway-obstructive from vascular causes, including chronic thromboembolic disease.

• Read the transplanted lung — integrate time since transplant and immunosuppression with the halo sign, the air-crescent sign, and the Pneumocystis pattern.

• Report it so the team can act — a five-element structured template and a cross-referenced atlas that turn every chapter into a two-minute lookup.

Open it before the next indeterminate case reaches your worklist.

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