LI-RADS 2018版在有肝癌病史的患者中的应用:LR4观察结果足以诊断复发性HCC吗?

Hee-Soo Kim, Joon-Il Choi, Bohyun Kim, Seo Yeon Youn, Hokun Kim, Dong Hwan Kim, S. Rha
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引用次数: 1

摘要

目的:我们评估LI-RADS 2018版使用加多乙酸增强MRI对有HCC病史的复发但未经治疗的HCC患者的诊断性能。材料和方法:我们连续招募了50例患者,他们1)既往有HCC治疗史,2)在2013年至2018年期间接受了肝脏手术以进行影像学/临床诊断为新发HCC, 3)术前一个月内进行了gadoxetic酸增强MRI检查,4)没有超过5个HCC或只有浸润性肿瘤。两名放射科医生审查了MRI,并确定了LR3、LR4和LR5的存在,除了之前治疗过的肿瘤,基于LI-RADS 2018版本的共识。我们将LR4细分为LR4m (LR4仅具有主要功能)和LR4u (LR4通过辅助功能从LR3升级)。LR4u进一步细分为LR4ua(动脉期高强化)和LR4un(无动脉期高强化)。结果:复发性HCC中LR5、LR4和LR3的PPV分别为100%、61.5%和25.0%。100%(3/3)的LR4m为HCC。而LR4u的PPV为56.5%。LR4ua和LR4un的PPV分别为73.3%和25.0%。LR5和LR5+LR4作为诊断阈值的敏感性分别为32.1%和89.3%。LR5+LR4m+LR4ua对HCC诊断的敏感性为83.7%,显著优于LR5,特异性无明显下降(75.0%)。结论:在既往有HCC病史的患者中,LR4的主要特征或APHE观察结果可被视为复发性HCC,因为LR5观察结果具有较高的敏感性和相当的特异性/PPV。
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LI-RADS version 2018 in Patients with Prior History of Hepatocellular Carcinoma: Are LR4 Observations Enough for the Diagnosis of Recurrent HCC?
Purpose: We evaluated the diagnostic performance of LI-RADS version 2018 using gadoxetic acid enhanced MRI for recurrent but untreated HCC in patients with prior history of HCC. Materials and Methods: We enrolled 50 consecutive patients who 1) prior history of treatment of HCC, 2) underwent liver surgery for radiological/clinical diagnosis of new HCC between 2013 to 2018, 3) had gadoxetic acid enhanced MRI within one month before surgery, and 4) did not have more than five HCCs or infiltrative tumors only. Two radiologists reviewed MRI and determined the presence of LR3, LR4 and LR5 observations except previously treated tumors based on LI-RADS version 2018 in consensus. We sub-classified LR4 into LR4m (LR4 with major features only) and LR4u (LR4 upgraded from LR3 by ancillary features). LR4u were further sub-classified into LR4ua (with arterial phase hyperenhancement) and LR4un (without arterial phase hyperenhancement). Results: PPV for LR5, LR4 and LR3 observations for recurrent HCC were 100%, 61.5% and 25.0%, respectively. 100% (3/3) of LR4m were HCC. However, PPV of LR4u was 56.5%. PPV of LR4ua and LR4un were 73.3% and 25.0%, respectively. Sensitivity of LR5 and LR5+LR4 observations as a diagnostic threshold were 32.1% and 89.3%, respectively. Sensitivity for LR5+LR4m+LR4ua observations for diagnosis of HCC were 83.7% and significantly superior to that of LR5 without significant deterioration of specificity (75.0%). Conclusion: In patients with prior history of HCC, LR4 observations by major features or with APHE may be regarded as recurrent HCCs given high sensitivity and comparable specificity/PPV to LR5 observations.
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