亲爱的研友该休息了!由于当前在线用户较少,发布求助请尽量完整的填写文献信息,科研通机器人24小时在线,伴您度过漫漫科研夜!身体可是革命的本钱,早点休息,好梦!

Central Role of CT in Management of Pulmonary Fibrosis

医学 肺纤维化 纤维化 放射科 内科学
作者
Kum Ju Chae,Hye Jeon Hwang,Rosane Duarte Achcar,J. Cooley,Stephen M. Humphries,Seth Kligerman,David A. Lynch
出处
期刊:Radiographics [Radiological Society of North America]
卷期号:44 (6)
标识
DOI:10.1148/rg.230165
摘要

With the approval of antifibrotic medications to treat patients with idiopathic pulmonary fibrosis and progressive pulmonary fibrosis, radiologists have an integral role in diagnosing these entities and guiding treatment decisions. CT features of early pulmonary fibrosis include irregular thickening of interlobular septa, pleura, and intralobular linear structures, with subsequent progression to reticular abnormality, traction bronchiectasis or bronchiolectasis, and honeycombing. CT patterns of fibrotic lung disease can often be reliably classified on the basis of the CT features and distribution of the condition. Accurate identification of usual interstitial pneumonia (UIP) or probable UIP patterns by radiologists can obviate the need for a tissue sample-based diagnosis. Other entities that can appear as a UIP pattern must be excluded in multidisciplinary discussion before a diagnosis of idiopathic pulmonary fibrosis is made. Although the imaging findings of nonspecific interstitial pneumonia and fibrotic hypersensitivity pneumonitis can overlap with those of a radiologic UIP pattern, these entities can often be distinguished by paying careful attention to the radiologic signs. Diagnostic challenges may include misdiagnosis of fibrotic lung disease due to pitfalls such as airspace enlargement with fibrosis, paraseptal emphysema, recurrent aspiration, and postinfectious fibrosis. The radiologist also plays an important role in identifying complications of pulmonary fibrosis-pulmonary hypertension, acute exacerbation, infection, and lung cancer in particular. In cases in which there is uncertainty regarding the clinical and radiologic diagnoses, surgical biopsy is recommended, and a multidisciplinary discussion among clinicians, radiologists, and pathologists can be used to address diagnosis and management strategies. This review is intended to help radiologists diagnose and manage pulmonary fibrosis more accurately, ultimately aiding in the clinical management of affected patients.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
大幅提高文件上传限制,最高150M (2024-4-1)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
lxseva完成签到 ,获得积分10
刚刚
陈雨发布了新的文献求助10
4秒前
5秒前
yaya完成签到 ,获得积分10
7秒前
14秒前
木又完成签到 ,获得积分10
18秒前
18秒前
20秒前
虚幻幻然完成签到 ,获得积分10
21秒前
ZHAOyifan发布了新的文献求助10
30秒前
勤劳的冰菱完成签到,获得积分10
54秒前
慕青应助麻绳青年采纳,获得10
56秒前
wanci应助科研通管家采纳,获得10
58秒前
无花果应助科研通管家采纳,获得10
58秒前
59秒前
情怀应助科研通管家采纳,获得10
59秒前
abiorz完成签到,获得积分10
1分钟前
窗外是蔚蓝色完成签到,获得积分10
1分钟前
单薄的酬海关注了科研通微信公众号
1分钟前
Wilson完成签到 ,获得积分10
1分钟前
Perion完成签到 ,获得积分10
1分钟前
vuig完成签到 ,获得积分10
1分钟前
哈哈哈哈完成签到 ,获得积分10
1分钟前
June完成签到 ,获得积分10
1分钟前
Harlotte完成签到 ,获得积分10
1分钟前
蚂蚁踢大象完成签到 ,获得积分10
1分钟前
liuqi完成签到 ,获得积分10
1分钟前
1分钟前
麻绳青年发布了新的文献求助10
1分钟前
1分钟前
麻绳青年完成签到,获得积分10
2分钟前
2分钟前
高鑫完成签到 ,获得积分10
2分钟前
喜遇徐完成签到 ,获得积分10
2分钟前
gy完成签到,获得积分10
2分钟前
Wei_eas完成签到,获得积分10
2分钟前
Wei_eas发布了新的文献求助10
2分钟前
jiafang完成签到,获得积分10
2分钟前
LaiDa229完成签到,获得积分10
2分钟前
甜甜盼夏发布了新的文献求助10
2分钟前
高分求助中
LNG地下式貯槽指針(JGA Guideline-107)(LNG underground storage tank guidelines) 1000
Generalized Linear Mixed Models 第二版 1000
rhetoric, logic and argumentation: a guide to student writers 1000
QMS18Ed2 | process management. 2nd ed 1000
Asymptotically optimum binary codes with correction for losses of one or two adjacent bits 800
Preparation and Characterization of Five Amino-Modified Hyper-Crosslinked Polymers and Performance Evaluation for Aged Transformer Oil Reclamation 700
Operative Techniques in Pediatric Orthopaedic Surgery 510
热门求助领域 (近24小时)
化学 医学 材料科学 生物 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 基因 遗传学 物理化学 催化作用 免疫学 细胞生物学 电极
热门帖子
关注 科研通微信公众号,转发送积分 2924250
求助须知:如何正确求助?哪些是违规求助? 2569997
关于积分的说明 6944119
捐赠科研通 2224254
什么是DOI,文献DOI怎么找? 1182365
版权声明 589020
科研通“疑难数据库(出版商)”最低求助积分说明 578547