• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

间质性肺疾病的临床处理方法

Clinical approach to interstitial lung disease.

作者信息

Scholand Mary Beth

机构信息

Pulmonary Division, University of Utah, 26 North 1900 East, Salt Lake City, UT 84112, USA.

出版信息

Semin Ultrasound CT MR. 2002 Aug;23(4):269-74. doi: 10.1016/s0887-2171(02)90016-8.

DOI:10.1016/s0887-2171(02)90016-8
PMID:12465684
Abstract

The term interstitial lung disease (ILD) encompasses a large variety of entities. The clinical diagnosis is often difficult and is a multidisciplinary process. Achieving the correct diagnosis often involves 3 elements: a clinical impression, radiologic evaluation, and a pathologic opinion. All 3 components play a critical role. Frequently, the goal is differentiating idiopathic pulmonary fibrosis (IPF) from more treatable entities. This article provides an overview of the input provided by the 3 specialties cited earlier, as well as the interrelationship among these specialties in the diagnosis of ILD. Additional consideration is given to the decision-making process involved in determining when to obtain a biopsy specimen from a patient with ILD, and a review of current treatment strategies.

摘要

间质性肺疾病(ILD)这一术语涵盖了多种病症。临床诊断往往颇具难度,是一个多学科的过程。做出正确诊断通常涉及三个要素:临床印象、影像学评估以及病理诊断意见。这三个组成部分都起着关键作用。通常,目标是将特发性肺纤维化(IPF)与更具可治性的病症区分开来。本文概述了上述三个专业领域所提供的信息,以及这些专业领域在ILD诊断中的相互关系。此外,还考虑了决定何时对ILD患者进行活检标本采集的决策过程,并对当前的治疗策略进行了综述。

相似文献

1
Clinical approach to interstitial lung disease.间质性肺疾病的临床处理方法
Semin Ultrasound CT MR. 2002 Aug;23(4):269-74. doi: 10.1016/s0887-2171(02)90016-8.
2
Differentiating between IPF and NSIP.特发性肺纤维化和非特异性间质性肺炎的鉴别诊断。
Chron Respir Dis. 2010 Aug;7(3):187-95. doi: 10.1177/1479972310376205.
3
[Interstitial lung diseases].[间质性肺疾病]
Recenti Prog Med. 2003 May;94(5):227-37.
4
[Diagnosis and therapy of interstitial lung diseases].[间质性肺疾病的诊断与治疗]
Dtsch Med Wochenschr. 2009 Mar;134(11):524-9. doi: 10.1055/s-0029-1208082. Epub 2009 Mar 3.
5
The accuracy of the clinical diagnosis of new-onset idiopathic pulmonary fibrosis and other interstitial lung disease: A prospective study.新发特发性肺纤维化及其他间质性肺疾病临床诊断的准确性:一项前瞻性研究。
Chest. 1999 Nov;116(5):1168-74. doi: 10.1378/chest.116.5.1168.
6
Predictors of idiopathic pulmonary fibrosis in absence of radiologic honeycombing: A cross sectional analysis in ILD patients undergoing lung tissue sampling.无放射学蜂窝状改变的特发性肺纤维化的预测因素:对接受肺组织采样的间质性肺疾病患者的横断面分析
Respir Med. 2016 Sep;118:88-95. doi: 10.1016/j.rmed.2016.07.016. Epub 2016 Jul 28.
7
Long-term clinical course of anti-glycyl tRNA synthetase (anti-EJ) antibody-related interstitial lung disease pathologically proven by surgical lung biopsy.经外科肺活检病理证实的抗甘氨酰tRNA合成酶(抗EJ)抗体相关间质性肺疾病的长期临床病程
BMC Pulm Med. 2016 Dec 1;16(1):168. doi: 10.1186/s12890-016-0325-y.
8
Clinical profile of unclassifiable interstitial lung disease: Comparison with chronic fibrosing idiopathic interstitial pneumonias.无法分类的间质性肺疾病的临床特征:与慢性纤维化性特发性间质性肺炎的比较。
J Int Med Res. 2018 Jan;46(1):448-456. doi: 10.1177/0300060517719767. Epub 2017 Jul 31.
9
Cellular vs fibrosing interstitial pneumonias and prognosis: a practical classification of the idiopathic interstitial pneumonias and pathologically/radiologically similar conditions.细胞性与纤维化间质性肺炎及预后:特发性间质性肺炎及病理/放射学相似病症的实用分类
Chest. 2006 Nov;130(5):1566-70. doi: 10.1378/chest.130.5.1566.
10
Prevalence and prognosis of unclassifiable interstitial lung disease.无法分类的间质性肺疾病的患病率和预后。
Eur Respir J. 2013 Sep;42(3):750-7. doi: 10.1183/09031936.00131912. Epub 2012 Dec 6.