Diagnosis of idiopathic pulmonary fibrosis-the new guidelines

被引：0

作者：

Koschel, D. ^{[1
,2
]}

机构：

[1] Fachkrankenhaus Coswig, Lungenzentrum, Abt Innere Med & Pneumol, Coswig, Germany

[2] Tech Univ Dresden, Univ Klinikum Carl Gustav Carus, Med Klin Bereich Pneumol 1, Fetscherstr 74, D-01307 Dresden, Germany

来源：

PNEUMOLOGE | 2020年 / 17卷 / 03期

关键词：

Interstitial lung diseases; Usual interstitial pneumonia pattern; High-resolution computed tomography; Cryobiopsy; Lung biopsy; INTERSTITIAL LUNG-DISEASE; CLINICAL-PRACTICE; SURVIVAL; MANAGEMENT; STATEMENT; MORTALITY; BIOPSY;

D O I：

10.1007/s10405-020-00315-8

中图分类号：

R56 [呼吸系及胸部疾病];

学科分类号：

摘要：

Idiopathic pulmonary fibrosis (IPF) is one of the most frequent interstitial lung diseases (ILD). The correct diagnosis of IPF is still challenging. Recently, two international recommendations for the diagnostics of IPF were published, which summarized the current state of knowledge. In particular, the necessary exclusion of other causes of ILD depends on the extent of diagnostic measures and on the experience of the attending physician. The critical importance of high-resolution computed tomography (HRCT) of the thorax is emphasized with the accurate description of specific HRCT patterns. Depending on this, the need for an additional lung tissue biopsy is defined with a corresponding description of specific histopathological patterns. A multidisciplinary discussion is necessary for making diagnostic decisions.

引用

页码：162 / 168

页数：7

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