Salvatore Mary, Smith Maxwell L
Department of Radiology, Icahn School of Medicine at Mount Sinai, New York, NY, United States of America.
Department of Laboratory Medicine and Pathology, Mayo Clinic, Scottsdale, AZ, United States of America.
Clin Imaging. 2018 Sep-Oct;51:332-336. doi: 10.1016/j.clinimag.2018.06.013. Epub 2018 Jun 27.
There are three major pathologic patterns of pulmonary fibrosis; usual interstitial pneumonia (UIP), nonspecific interstitial pneumonia (NSIP) and airway-centered fibrosis (ACF). These pathologic patterns correspond with radiographic patterns of UIP, NSIP, and chronic hypersensitivity pneumonitis (CHP). Previous studies have demonstrated that the radiologic diagnosis is correct approximately 50% of the time for these fibrotic lung diseases. Understanding the microscopic pathologic patterns that are recapitulated at a macroscopic level in the high resolution CT scan is key to radiologists' ability to correctly diagnose pulmonary fibrosis and thus improve patient outcomes with early diagnosis and avoidance of biopsy. We investigate the similarities between the pathology and radiology features of UIP, NSIP, and ACF.
普通型间质性肺炎(UIP)、非特异性间质性肺炎(NSIP)和气道中心性纤维化(ACF)。这些病理模式与UIP、NSIP和慢性过敏性肺炎(CHP)的影像学模式相对应。先前的研究表明,对于这些纤维化性肺病,放射学诊断大约只有50%的时间是正确的。了解在高分辨率CT扫描宏观层面上重现的微观病理模式是放射科医生正确诊断肺纤维化并从而通过早期诊断和避免活检改善患者预后能力的关键。我们研究UIP、NSIP和ACF的病理学和放射学特征之间的相似性。