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特发性肺纤维化。

Idiopathic Pulmonary Fibrosis.

出版信息

Radiol Technol. 2020 Mar;91(4):361-376.

Abstract

Idiopathic pulmonary fibrosis (IPF) is an uncommon and fatal lung disease that causes the lung tissue to become progressively stiff and scarred. It is a type of interstitial lung disease that radiographers might encounter on the job. Chest radiography and high-resolution computed tomography of the lungs are necessary for diagnosing and treating IPF. This article describes the suspected causes and usual progression of IPF, diagnostic techniques, treatments, and prognosis.

摘要

特发性肺纤维化(IPF)是一种罕见且致命的肺部疾病,会导致肺组织逐渐变硬和结疤。它是一种放射技师在工作中可能会遇到的间质性肺病。胸部 X 射线摄影和肺部高分辨率计算机断层扫描对于诊断和治疗 IPF 是必要的。本文描述了 IPF 的可疑病因和常见进展、诊断技术、治疗方法和预后。

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