Department of Radiology, The University of Chicago Medical Center, 5841 S. Maryland Avenue, Chicago, IL, 60637, USA.
Section of Pulmonary/Critical Care, Department of Medicine, The University of Chicago Medical Center, 5841 South Maryland Ave., Chicago, IL, 60637, USA.
Eur Radiol. 2021 Oct;31(10):7295-7302. doi: 10.1007/s00330-021-07861-6. Epub 2021 Apr 13.
To determine if a quantitative imaging variable (vessel-related structures [VRS]) could identify subjects with a non-IPF diagnosis CT pattern who were highly likely to have UIP histologically.
Subjects with a multidisciplinary diagnosis of interstitial lung disease including surgical lung biopsy and chest CT within 1 year of each other were included in the study. Non-contrast CT scans were analyzed using the Computer-Aided Lung Informatics for Pathology Evaluation and Rating (CALIPER) program, which quantifies the amount of various abnormal CT patterns on chest CT. Quantitative data were analyzed relative to pathological diagnosis as well as the qualitative CT pattern.
CALIPER-derived volumes of reticulation (p = 0.012), honeycombing (p = 0.017), and VRS (p < 0.001) were associated with a UIP pattern on pathology on univariate analysis but only VRS was associated with a UIP pathology on multivariable analysis (p = 0.013). Using a VRS cut-off of 173 cm, the sensitivity and specificity for pathological UIP were similar to those for standard qualitative CT assessment (55.9% and 80.4% compared to 60.6% and 80.4%, respectively). VRS differentiated pathological UIP cases in those with a non-IPF diagnosis CT category (p < 0.001) but not in other qualitative CT patterns (typical UIP, probable UIP, and indeterminate for UIP). The rate of pathological UIP in those with VRS greater than 173 cm (84.2%) was nearly identical to those who had a qualitative CT pattern of probable UIP (88.9%).
VRS may be an adjunct to CT in predicting pathology in patients with interstitial lung disease.
• Volume of vessel-related structures (VRS) was associated with usual interstitial pneumonia (UIP) on pathology. • This differentiation arose from those with CT scans with a non-IPF diagnosis imaging pattern. • Higher VRS has similar diagnostic ramifications for UIP as probable UIP, transitively suggesting in patients with high VRS, pathology may be obviated.
确定定量成像变量(与血管相关的结构 [VRS])是否可以识别具有非特发性肺纤维化(IPF)诊断 CT 模式的患者,这些患者极有可能具有组织学上的普通型间质性肺炎(UIP)。
本研究纳入了在 1 年内接受过多学科诊断为间质性肺疾病(包括外科肺活检和胸部 CT)的患者。使用计算机辅助肺病理学评估和评分(CALIPER)程序分析非对比 CT 扫描,该程序可定量评估胸部 CT 上各种异常 CT 模式的数量。定量数据相对于病理诊断和定性 CT 模式进行了分析。
在单变量分析中,CALIPER 得出的网状结构(p=0.012)、蜂窝状结构(p=0.017)和 VRS(p<0.001)体积与病理学上的 UIP 模式相关,但仅 VRS 与多变量分析中的 UIP 病理学相关(p=0.013)。使用 VRS 截断值 173cm,VRS 对 UIP 病理的敏感性和特异性与标准定性 CT 评估相似(分别为 55.9%和 80.4%,与 60.6%和 80.4%相比)。VRS 可区分具有非 IPF 诊断 CT 类别的患者的 UIP 病理(p<0.001),但不能区分其他定性 CT 模式(典型 UIP、可能 UIP 和 UIP 不确定)。VRS 大于 173cm 的患者中 UIP 病理的发生率(84.2%)与具有可能 UIP 定性 CT 模式的患者几乎相同(88.9%)。
VRS 可能是 CT 预测间质性肺疾病患者病理的辅助手段。
VRS 与病理学上的普通型间质性肺炎(UIP)相关。
这种差异来自于具有非特发性肺纤维化(IPF)诊断成像模式的 CT 扫描患者。
较高的 VRS 对 UIP 的诊断意义与可能的 UIP 相似,这意味着在 VRS 较高的患者中,可能可以避免进行病理学检查。