特发性肺纤维化:放射科医生的高分辨率CT指南

IF 0.1 Q4 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
Jamie Strike, Nicholas Organ, Nidhi Reddy, Monica Cooley, Cary Squires, Christopher Bennett, L. Lozano
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引用次数: 0

摘要

特发性肺纤维化(IPF)是一种病因不明的进行性、不可逆的肺纤维化。它被认为是最常见的特发性间质性肺炎,属于间质性肺病(ILD)的广泛类别。IPF在高分辨率CT上的主要影像学表现是典型的间质性肺炎(UIP)型。然而,一些影像学表现可能与其他ild和病症重叠,因此我们对这些标志性的表现和重叠的影像学表现进行了回顾。鉴于疾病的进行性和衰弱性,对于放射科医生来说,能够识别UIP的关键成像特征以帮助诊断IPF和早期开始治疗是很重要的,这已被证明可以保护肺功能并改善预后。第46卷•第7号www.cdrnewsletter.com 2023年3月31日
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Idiopathic Pulmonary Fibrosis: A Radiologist's Guide to High-resolution CT
Idiopathic pulmonary fibrosis (IPF) is a progressive, irreversible condition of unknown cause that results in pulmonary fibrosis. It is considered the most common idiopathic interstitial pneumonia, falling under the broad category of interstitial lung disease (ILD). The key imaging finding in IPF on high-resolution CT is the typical usual interstitial pneumonia (UIP) pattern. However, some of the imaging findings may overlap with other ILDs and conditions, so these hallmark findings and overlapping imaging findings have been reviewed. Given the progressive and debilitating nature of disease, it is important for the radiologist to be able to identify the key imaging characteristics of UIP to help aid in the diagnosis of IPF and early initiation of treatment, which has been shown to preserve lung function and improve outcomes. VOLUME 46 • NO 7 www.cdrnewsletter.com MARCH 31, 2023
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