Department of Radiodiagnosis and Imaging, Postgraduate Institute of Medical Education & Research, Chandigarh, India.
Department of Pulmonary Medicine, Postgraduate Institute of Medical Education & Research, Chandigarh, India.
JNMA J Nepal Med Assoc. 2024 Jul 31;62(276):511-515. doi: 10.31729/jnma.8706.
Idiopathic pulmonary fibrosis is the most prevalent form of interstitial lung disease, which presents as usual interstitial pneumonia on histopathology and imaging. It leads to significant lung scarring, damage, and fibrosis and is associated with a high degree of mortality, repeated hospital admissions, and oxygen dependence. Many complications are associated with idiopathic pulmonary fibrosis, which further increases the morbidity of patients. High-resolution computed tomography chest is the imaging modality of choice for usual interstitial pneumonia tracking its progression, evaluating treatment response, and detecting potential complications.
This descriptive cross-sectional study was approved by the Institutional Ethics Committee (Reference number: IEC-INT/2023/Study-1256). Departmental computed tomography report database from November, 2017 to June, 2018 was reviewed and scans with imaging features consistent with the 'usual interstitial pneumonia' pattern were identified. Total sampling method was used and two independent radiologists, blinded to the patient's clinical information, reviewed the high-resolution computed tomography chest scans to assess for imaging features of usual interstitial pneumonia and associated complications. Data was collected and analyzed using Microsoft Excel.
There were 65 patients reported as unusual interstitial pneumonia pattern. Emphysema and pneumothorax were identified in 4 (6.15%) and 1 (1.53%) scans, respectively. Two (3.08%) scans showed features of pulmonary arterial hypertension. Ten (15.38%) scans exhibited findings consistent with co-existent or superimposed pulmonary infection. Additionally, features of lung malignancy were identified in high-resolution computed tomography scans of 5 (7.69%) patients.
Patients with UIP often experience severe lung scarring, and frequent complications, and require regular chest CT scans to monitor disease progression and identify potential complications.
特发性肺纤维化是最常见的间质性肺疾病形式,组织病理学和影像学表现为寻常型间质性肺炎。它导致显著的肺瘢痕、损伤和纤维化,并与高死亡率、反复住院和氧依赖相关。特发性肺纤维化常伴有许多并发症,进一步增加了患者的发病率。高分辨率 CT 胸部扫描是寻常型间质性肺炎的首选影像学检查方法,用于跟踪其进展、评估治疗反应和检测潜在并发症。
这项描述性横断面研究得到了机构伦理委员会的批准(编号:IEC-INT/2023/Study-1256)。回顾了 2017 年 11 月至 2018 年 6 月的部门 CT 报告数据库,并识别出具有与“寻常型间质性肺炎”模式一致的影像学特征的扫描。采用完全抽样法,两名独立的放射科医生在不了解患者临床信息的情况下,对高分辨率 CT 胸部扫描进行评估,以评估寻常型间质性肺炎的影像学特征和相关并发症。使用 Microsoft Excel 收集和分析数据。
有 65 例报告为不寻常型间质性肺炎模式。分别在 4 例(6.15%)和 1 例(1.53%)扫描中发现肺气肿和气胸。2 例(3.08%)扫描显示肺动脉高压特征。10 例(15.38%)扫描显示与共存或重叠性肺部感染一致的发现。此外,在 5 例(7.69%)患者的高分辨率 CT 扫描中发现了肺癌的特征。
UIP 患者常经历严重的肺瘢痕和频繁的并发症,需要定期进行胸部 CT 扫描,以监测疾病进展和识别潜在并发症。