CT imaging findings of renal epithelioid lipid-poor angiomyolipoma

医学 神经组阅片室 逻辑回归 放射科 置信区间 血管平滑肌脂肪瘤 介入放射学 超声波 磁共振成像 内科学 神经学 精神科
作者
Di Wang,Guanghui Gong,Yan Fu,Liping Zhu,Hongling Yin,Longfei Liu,Zhiming Zhu,Gaofeng Zhou,Ang Yan,Guangwu Lei,Changyong Chen,Peipei Pang,Xiaoping Yi,Yehong Kuang,Bihong T. Chen
出处
期刊:European Radiology [Springer Nature]
卷期号:32 (7): 4919-4930 被引量:2
标识
DOI:10.1007/s00330-021-08528-y
摘要

ObjectivesTo identify specific imaging and clinicopathological features of a rare potentially malignant epithelioid variant of renal lipid-poor angiomyolipoma (E-lpAML).MethodsA total of 20 patients with E-lpAML and 43 patients with other lpAML were retrospectively included. Multiphase computed tomography (CT) imaging features and clinicopathological findings were recorded. Independent predictors for E-lpAML were identified using multivariate logistic regression and were used to construct a diagnostic score for differentiation of E-lpAML from other lpAML.ResultsThe E-lpAML group consisted of 6 men and 14 women (age median ± SD: 39.45 ± 15.70, range: 16.0–68.0 years). E-lpAML tended to appear as hyperdense mass lesions located at the renal sinus (n = 8, 40%) or at the renal cortex (n = 12, 60%), with a “fast-in and slow-out” enhancement pattern (n = 20, 100%), cystic degeneration (n = 18, 90%), “eyeball” sign (n = 11, 55%), and tumor neo-vasculature (n = 15, 75%) on CT. Multivariate logistic regression analysis showed that the independent predictors for diagnosing E-lpAML were cystic degeneration on CT imaging and CT value of the tumor in corticomedullary phase of enhancement. A predictive model was built with the two predictors, achieving an area under the curve (AUC) of 93.5% (95% confidence interval (95%CI): 84.3–98.2%) with a sensitivity of 95.0% (95%CI: 75.1–99.9%) and a specificity of 83.72% (95%CI: 69.3–93.2%).ConclusionWe identified specific CT imaging features and predictors that could contribute to the correct diagnosis of E-lpAML. Our findings should be helpful for clinical management of E-lpAML which could potentially be malignant and may require nephron-sparing surgery while other lpAML tumors which are benign require no intervention.Key Points• It is important to differentiate renal epithelioid lipid-poor angiomyolipoma (E-lpAML) from other lpAML because of differences in clinical management.• E-lpAML tumors tend to be large hyperdense tumors in the renal sinus with cystic degeneration and “fast-in and slow-out” pattern of enhancement.• Our CT imaging-based predictive model was robust in its performance for predicting E-lpAML from other lpAML tumors.
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