We read with great enthusiasm the Review¹ published by David Lynch and colleagues, and we congratulate the authors for the magnificent manuscript. The authors provided an updated approach to the diagnosis of idiopathic pulmonary fibrosis (IPF), representing the expert opinion of members of the Fleischner Society. When compared with previous ATS/ERS official documents,^2,3 the role of high-resolution CT is expanded to permit diagnosis of IPF without surgical biopsy in cases showing a probable usual interstitial pneumonia (UIP) pattern.

中文翻译：

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特发性肺纤维化的诊断标准

我们以极大的热情阅读了大卫·林奇（David Lynch）及其同事发表的《评论¹》，并祝贺作者们手稿精美。作者提供了一种更新的方法来诊断特发性肺纤维化（IPF），代表了Fleischner Society成员的专家意见。与以前的ATS / ERS官方文件相比，^2,3扩大了高分辨率CT的作用，从而在显示可能的普通间质性肺炎（UIP）模式的情况下，无需手术活检即可诊断IPF。