Abstract
Diffuse parenchymal lung diseases (DPLDs) encompass a variety of restrictive and obstructive lung pathologies. In this article, the authors discuss a series of rare pulmonary entities and their high-resolution computed tomography imaging appearances, which can mimic more commonly encountered patterns of DPLDs. These cases highlight the importance of surgical lung biopsies in patients with imaging findings that do not show typical imaging features of usual interstitial pneumonia.
Original language | English (US) |
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Pages (from-to) | 231-236 |
Number of pages | 6 |
Journal | Lung India |
Volume | 35 |
Issue number | 3 |
DOIs | |
State | Published - May 1 2018 |
Keywords
- Amyloidosis
- diffuse idiopathic pulmonary neuroendocrine cell hyperplasia
- pleuroparenchymal fibroelastosis
- pulmonary capillary hemangiomatosis
- usual interstitial pneumonia
ASJC Scopus subject areas
- Pulmonary and Respiratory Medicine