肺间质纤维化影像学表型的频率。

IF 0.9 Q4 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
SA Journal of Radiology Pub Date : 2025-05-09 eCollection Date: 2025-01-01 DOI:10.4102/sajr.v29i1.3098
Wallace T Miller, Scott Simpson, Shweta Sood, Michelle Hershman, Cheilonda R Johnson, James E Schmitt, Karen C Patterson
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引用次数: 0

摘要

背景:弥漫性间质性肺疾病(ILD)的胸部影像学评价比较复杂。放射科医生经常使用一种模式方法来解释;然而,他们很少意识到疾病呈现的统计频率。目的:评价纤维化性ILD病因的相对频率与影像学模式的关系。方法:从机构弥漫性肺疾病登记和回顾性医疗记录中收集396例纤维化ILD的CT数据库。三名放射科医生和一名肺科医生独立和盲目地审查了CT扫描的纤维化分布,主要特征和非肺部发现。结果:外周纤维化最常见(291/396,73.5%),通常由特发性肺纤维化(IPF)和结缔组织病相关间质性肺病(CTD-ILD)引起,但偶尔由超敏性肺炎(HP)、特发性非特异性间质性肺炎(iNSIP)和石棉肺引起。周围纤维化伴蜂窝状通常为IPF,无蜂窝状通常为CTD-ILD。周围纤维化伴胸膜斑块均为石棉肺。周围纤维化伴食管扩张多为结缔组织疾病。实变样外周纤维化为CTD-ILD。轴向纤维化(61/396,15.4%)多为结节病、HP、CTD-ILD或矽肺。轴性纤维化以实变样纤维化、蜂窝状纤维化或网状纤维化为主,通常为结节病。以磨玻璃混浊为主的轴性纤维化常为HP或CTD-ILD。淋巴结钙化或短轴> 17mm增加结节病引起轴性纤维化的可能性。非特异性纤维化表型不常见(44/396,11.1%),通常为CTD-ILD(25/44, 57%),但也有HP、IPF、iNSIP或石棉肺。结论:肺纤维化的模式为确定病因提供了指导。贡献:预测10种ILD类型病因相对频率的流程图。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Frequency of imaging phenotypes of pulmonary interstitial fibrosis.

Frequency of imaging phenotypes of pulmonary interstitial fibrosis.

Frequency of imaging phenotypes of pulmonary interstitial fibrosis.

Frequency of imaging phenotypes of pulmonary interstitial fibrosis.

Background: Evaluation of diffuse interstitial lung disease (ILD) in thoracic imaging is complicated. Radiologists often use a pattern approach to interpretation; however, they are rarely aware of the statistical frequency of disease presentation.

Objectives: To evaluate the relative frequency of causes of fibrotic ILD as a function of imaging patterns.

Method: A CT database of 396 cases of fibrotic ILD was amassed from an institutional diffuse lung disease registry and retrospective search of medical records. Three radiologists and one pulmonologist independently and blindly reviewed the CT scans for the distribution of fibrosis, predominant feature and non-pulmonary findings.

Results: Peripheral fibrosis was most common (291/396, 73.5%), usually caused by idiopathic pulmonary fibrosis (IPF) and connective tissue diseases-related interstitial lung disease (CTD-ILD) but occasionally by hypersensitivity pneumonitis (HP), idiopathic nonspecific interstitial pneumonia (iNSIP) and asbestosis. Peripheral fibrosis with honeycombing was usually IPF and without honeycombing, was usually CTD-ILD. Peripheral fibrosis with pleural plaques was always asbestosis. Peripheral fibrosis with oesophageal dilatation was usually connective tissue diseases. Consolidative-like peripheral fibrosis was CTD-ILD. Axial fibrosis (61/396, 15.4%) was usually sarcoidosis, HP, CTD-ILD or silicosis. Axial fibrosis with predominantly consolidative-like fibrosis, honeycombing, or reticulation was usually sarcoidosis. Axial fibrosis predominated by ground glass opacity was usually HP or CTD-ILD. Lymph node calcification or short axis > 17 mm increased the probability that axial fibrosis was due to sarcoidosis. The non-specific fibrosis phenotype was uncommon (44/396, 11.1%), usually CTD-ILD (25/44, 57%) but also HP, IPF, iNSIP or asbestosis.

Conclusion: Patterns of lung fibrosis provide guidelines to identify the cause.

Contribution: A flow diagram that predicts the relative frequency of the causes of 10 patterns of ILD.

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来源期刊
SA Journal of Radiology
SA Journal of Radiology RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING-
CiteScore
1.20
自引率
11.10%
发文量
35
审稿时长
16 weeks
期刊介绍: The SA Journal of Radiology is the official journal of the Radiological Society of South Africa and the Professional Association of Radiologists in South Africa and Namibia. The SA Journal of Radiology is a general diagnostic radiological journal which carries original research and review articles, pictorial essays, case reports, letters, editorials, radiological practice and other radiological articles.
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