目前特发性肺纤维化与纤维化性过敏性肺炎的组织病理学分离的可能性。怎么做呢?

Q4 Medicine
Ceskoslovenska patologie Pub Date : 2023-01-01
Radoslav Matěj
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引用次数: 0

摘要

进行性肺纤维化的组织病理学模式可以在许多不同的纤维化性肺间质性疾病中看到。准确的诊断是精确治疗的关键,而且不同的疾病有不同的预后。该组中最重要的疾病是特发性肺纤维化和纤维化过敏性肺炎,由于患者的治疗方法完全不同,因此将它们分开是至关重要的。本文的目的是总结常见间质性肺炎、特发性肺纤维化和纤维化性超敏性肺炎的最重要特征,并在多学科团队有效合作的框架下为这些疾病的精确诊断提供实用的工作。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Current possibilities of histopathologic separation of idiopathic pulmonary fibrosis from fibrotic hypersensitivity pneumonitis. How to do it?

Histopathological pattern of progressive pulmonary fibrosis could be seen in many different fibrotic lung interstitial diseases. Exact diagnosis is crucial for precise therapy, moreover, different diseases have different prognosis. The most important disorders in this group are idiopatic pulmonary fibrosis and fibrotic hypersensitivity pneumonitis, and their separation is crucial because of totally different treatment of the patients. The aim of this review is to sum up the most important characteristics of usual interstitial pneumonia, histopathological pattern of idiopatic pulmonary fibrosis, and fibrotic hypersensitivity pneumonitis and provide a practical work-up for precise diagnostics of these diseases in the frame of effectively cooperating multidisciplinary team.

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来源期刊
Ceskoslovenska patologie
Ceskoslovenska patologie Medicine-Medicine (all)
CiteScore
0.40
自引率
0.00%
发文量
17
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