| 摘要: |
| ［摘要］ 特发性肺纤维化（idiopathic pulmonary fibrosis，IPF）是一种慢性进行性纤维化性间质性肺炎，组织学和胸部高分辨率CT（high-resolution CT，HRCT）表现为普通型间质性肺炎（usual interstitial pneumonia，UIP）。Fleischner协会新发表了关于IPF的HRCT诊断标准，将原先2011年美国胸科学会（American Thoracic Society，ATS）、欧洲呼吸学会（European Respiratory Society，ERS）、日本呼吸学会（Japanese Respiratory Society，JRS）和拉丁美洲胸科学会（Latin American Thoracic Association，ALAT）制定的指南中可能UIP型更名为很可能UIP型，为临床医师提供了更为简洁的IPF临床诊断方式。 |
| 关键词: 特发性肺纤维化 高分辨率CT 诊断 Fleischner协会 |
| DOI：10.3969/j.issn.1674-3806.2019.01.04 |
| 分类号:R 563.13 |
| 基金项目:国家自然科学基金面上项目（编号：81670058）；江苏省科技厅重点研发项目（编号：BE2016611） |
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| New insight in HRCT diagnosis of idiopathic pulmonary fibrosis |
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LIU Yin, CAI Hou-rong
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Department of Respiratory Medicine, Nanjing Drum Tower Hospital Affiliated to Medical College of Nanjing University, Jiangsu 210009, China
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| Abstract: |
| ［Abstract］ Idiopathic pulmonary fibrosis(IPF) is a chronic progressive fibrosing interstitial pneumonia. It is a distinct clinical entity associated with the histologic and high-resolution CT(HRCT) appearance of usual interstitial pneumonia(UIP). The Fleischner Society provides an updated approach to the HRCT diagnosis of IPF. The possible UIP pattern, according to the 2011 ATS/ERS/JRS/ALAT guidelines, has been upgraded to a probable UIP pattern, which will contribute to providing clinicans with a more simple and straightforward clinical diagnosis of IPF. |
| Key words: Idiopathic pulmonary fibrosis High-resolution CT Diagnosis The Fleischner Society |
