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DOI 10.1038/s41598-025-91902-3

Медицинская библиотека · Scientific reports · 2025

Correlation between imaging features of pure ground-glass opacities and pathological subtypes of lung minimally invasive adenocarcinoma and precursor lesions.

Zhu Yanqiu, Yan Cui, Tang Wenjie, Duan Yani, Chen Xiuzhen, Dong Yunxu, Guo Yuefei, Liu Weimin, Qin Jie

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Аннотация

This study aimed to investigate the relationship between imaging features of pure ground-glass opacities (pGGOs) and the pathological subtypes of minimally invasive adenocarcinoma (MIA) and precursor lesions. A retrospective analysis was conducted on data from 1521 patients diagnosed with GGOs as lung adenocarcinoma or precursor lesions between January 2015 and March 2021. The pGGOs were categorized into atypical adenomatous hyperplasia (AAH) / adenocarcinoma in situ (AIS) and MIA groups. Clinical information and CT imaging features were collected. Statistical analysis, logistic regression, and receiver operating characteristic (ROC) curve analysis were performed. A total of 127 patients with 139 pGGOs were included. Maximum radiodensity, minimum radiodensity, mean radiodensity, variance, and skewness showed significant differences between the two groups. Maximum radiodensity and maximum cross-sectional area were identified as risk factors for pathology. The logistic regression model yielded an area under the curve (AUC) of 0.747 (95% CI, 0.666-0.816) for predicting pathological subtypes. The intensity features of pGGOs were found to be significantly different between AAH/AIS and MIA groups. Maximum radiodensity and skewness were independent risk factors for pathology. However, these features did not exhibit satisfactory diagnostic efficiency.

Для цитирования: Zhu Yanqiu, Yan Cui, Tang Wenjie, Duan Yani, Chen Xiuzhen, Dong Yunxu, Guo Yuefei, Liu Weimin, Qin Jie. Correlation between imaging features of pure ground-glass opacities and pathological subtypes of lung minimally invasive adenocarcinoma and precursor lesions.. Scientific reports. 2025. DOI: 10.1038/s41598-025-91902-3.

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