实用肝脏病杂志 ›› 2026, Vol. 29 ›› Issue (3): 409-412.doi: 10.3969/j.issn.1672-5069.2026.03.023

• 肝癌 • 上一篇    下一篇

双表型肝细胞癌患者增强磁共振成像表现特征分析*

王立峰, 李岩, 刘翠翠, 袁德昌, 许春苗, 陈学军, 韩帅   

  1. 450008 河南省郑州市 郑州大学附属肿瘤医院/河南省肿瘤医院医学影像科(王立峰,刘翠翠,袁德昌,许春苗,陈学军,韩帅);微创介入科(李岩)
  • 收稿日期:2025-11-07 出版日期:2026-05-10 发布日期:2026-05-18
  • 通讯作者: 陈学军,E-mail:chenxuejun1967@163.com
  • 作者简介:王立峰,男,38岁,医学硕士,主治医师。E-mail:leifwang@163.com
  • 基金资助:
    *河南省医学科技攻关计划项目(编号:LHGJ20230105)

Enhanced magnetic resonance imaging features of patients with biphenotypic hepatocellular carcinoma

Wang Lifeng, Li Yan, Liu Cuicui, et al   

  1. Department of Radiology, Provincial Tumor Hospital, Affiliated to Zhengzhou University, Zhengzhou 450008, Henan Province, China
  • Received:2025-11-07 Online:2026-05-10 Published:2026-05-18

摘要: 目的 分析双表型肝细胞癌(BPHCC)患者增强磁共振成像(MRI)表现特征。方法 2019年1月~2023年10月我院诊治的50例BPHCC患者,均接受钆塞酸二钠(Gd-EOB-DTPA)增强MR扫描,记录动脉期病灶-肝脏信号比 SIR-AP)、门脉期病灶-肝脏信号比 (SIR-PP)、移行期病灶-肝脏信号比 (SIR-EP)、肝胆期病灶-肝脏信号比 (SIR-HBP)和动脉期对比增强比 (CER-AP)。取术后组织行病理学检查诊断微血管侵犯(pMVI),采用多因素Logistic回归分析影响因素。结果 中高分化和pMVI阴性BPHCC在MRI上表现为边界较清晰的结节,动脉期病灶呈不均匀强化,在肝胆期呈特征性低信号,而低分化和pMVI阳性肿瘤常常肿瘤体积更大、边缘不光滑、动脉期可见瘤周强化,而在门脉期和移行期呈相对强度较低信号;在本组50例BPHCC患者中,病理学检查发现pMVI阳性者14例,pMVI阴性者36例;pMVI阳性组血清甲胎蛋白(AFP)水平、肿瘤大小、Edmondson-Steiner Ⅲ级、增强扫描动脉期瘤周强化和马赛克征占比分别为(421.2±123.7)ng/ml、(7.1±0.9)cm、42.9%、42.9%和35.7%,均显著大于或高于pMVI阴性组【分别为(311.6±127.6)ng/ml、(3.8±0.6)cm、19.4%、11.1%和19.4%,P<0.05】;pMVI阳性肿瘤SIR-PP和SIR-EP水平分别为(0.8±0.2)和(0.8±0.2),均显著低于pMVI阴性肿瘤【分别为(1.1±0.2)和(1.0±0.1), P<0.05】;多因素Logistic回归分析显示,增强MR扫描肿瘤SIR-PP【OR: 2.7(95% CI:1.2~6.2)】和动脉期瘤周强化【OR: 3.6(95% CI:1.4~9.6)】为提示pMVI阳性BPHCC的因素(P<0.05)。结论 BPHCC 肿瘤在增强MRI上无特殊表现,也可出现pMVI,其临床意义还需要进一步探讨。

关键词: 双表型肝细胞癌, 钆塞酸二钠, 磁共振成像, 门脉期病灶-肝脏信号比, 移行期病灶-肝脏信号比, 微血管侵犯, 分化

Abstract: Objective This study was to summarize enhanced magnetic resonance imaging (MRI) features of patients with biphenotypic hepatocellular carcinoma (BPHCC). Methods 50 patients with BPHCC were encountered in our hospital between January 2019 and October 2023, and the diagnosis and pathological microvascular invasion (pMVI) were determined by histo-pathological examination. All patients underwent gadolinium disulfide (Gd-EOB-DTPA) enhancement scan to record signal intensity ratio in arterial phase (SIR-AP), signal intensity ratio in portal venous phase (SIR-PP), signal intensity ratio in transitional phase (SIR-EP), signal intensity ratio in hepatobiliary phase (SIR-HBP) and contrast enhancement ratio in arterial phase (CER-AP). Multivariate Logistic regression analysis was applied to find factors that hinted pMVI positive. Results Well-differentiated and pMVI negative BPHCC presented as lesions with distinct edges on MRI, heterogeneous enhancement in arterial phase and low signals in hepatobiliary phase, while poorly-differentiated and pMVI positive tumors exhibited large tumor volume, vague edges, peri-tumor enhancement in arterial phase, with low signals in portal and in equilibrium phase; of the 50 patients with BPHCC, histo-pathological examination found pMVI positive in 14 cases and pMVI negative in 36 cases; serum alpha-fetoprotein (AFP) level, tumor size, percentages of Edmondson-Steiner stage Ⅲ, peri-tumor enhancement in arterial phase and Mosaic signs in pMVI positive tumor were (421.2±123.7)ng/ml, (7.1±0.9)cm, 42.9%, 42.9% and 35.7%, all much greater or higher than [(311.6±127.6)ng/ml, (3.8±0.6)cm, 19.4%, 11.1% and 19.4%, respectively, P<0.05] in pMVI negative tumor; SIR-PP and SIR-EP in pMVI positive tumor were (0.8±0.2) and (0.8±0.2), both significantly lower than [(1.1±0.2) and (1.0±0.1), respectively, P<0.05] in pMVI negative tumor; multivariate Logistic regression analysis showed that SIR-PP[OR: 2.7(95% CI:1.2-6.2)] and peri-tumor enhancement in arterial phase [OR: 3.6(95% CI:1.4-9.6)] were the independent factors suggesting pMVI positive in patients with BPHCC(P<0.05). Conclusion We don’t find special imaging features of patients with BPHCC, who might have early pMVI positive lesions, which needs further studies pathologically and clinically.

Key words: Biphenotypic hepatocellular carcinoma, Disodium gadolinate, Magnetic resonance imaging, Signal intensity ratio in portal venous phase, Signal intensity ratio in transitional phase, Microvascular invasion, Differentiation