Department of Radiology, Gifu University Hospital, 1-1 Yanagido, Gifu 501-1193, Japan.
Eur J Radiol. 2011 Aug;79(2):e108-12. doi: 10.1016/j.ejrad.2011.04.041. Epub 2011 May 17.
To retrospectively assess imaging features that help differentiate early-enhancing non-tumorous (EN) hepatic lesions from hepatocellular carcinomas (HCCs) on gadoxetate disodium-enhanced MR imaging.
Our institutional review board approved this retrospective study. We reviewed the studies of 158 patients (92 men and 65 women; age range: 29-91; mean age: 65.6 years) with chronic liver damage, who underwent gadoxetate disodium-enhanced MR imaging at 3T MR scanner. Hypervascular lesions identified during the hepatic artery phase were selected for a study cohort. The location, shape, size (maximum diameter and maximum area), and contrast enhancement signal intensity characteristics of the lesions were evaluated, then compared between the EN and HCC lesions.
A total of 65 EN lesions (range: 3-60mm, mean: 13.6 ± 10.6 mm) from 35 patients and 33 HCCs (range: 9-61 mm, mean: 19.3 ± 12.6 mm) from 20 patients were identified. Lesions were more frequently round or oval in shape for HCCs (n=29; 88%) than ENs (n=26; 40%) (P<0.01). Unexpectedly, some ENs (n=12; 18%) showed hypointensity on hepatocyte-phase, and 6 (50%) of them were T2 hyperintense. For lesions smaller than 2 cm (9 ENs and 21 HCCs) on hepatic arterial-phase images, the mean area of hypointensity in hepatocyte-phase (54.2 ± 33.1 mm(2)) was significantly smaller than those of the corresponding hyperintensity in hepatic arterial-phase (97.1 ± 42.0 mm(2)) for EN lesions (P=0.019), whereas no significant difference in area was found for HCCs.
EN lesions may occasionally present with hypointensity during the hepatocyte-phase; presenting a diagnostic dilemma. In this situation, EN lesions may be differentiated from HCCs when a hypointense area in hepatocyte-phase is smaller than the corresponding hypervascular area in hepatic-arterial phase.
回顾性分析钆塞酸二钠增强磁共振成像( gadoxetate disodium-enhanced MR imaging)中有助于鉴别早期强化非肿瘤性(EN)肝病变与肝细胞癌(HCC)的影像学特征。
本机构审查委员会批准了这项回顾性研究。我们对在 3T MR 扫描仪上进行钆塞酸二钠增强磁共振成像的 158 例慢性肝损伤患者(92 名男性和 65 名女性;年龄范围:29-91 岁;平均年龄:65.6 岁)的研究进行了回顾。选择肝动脉期发现的富血管性病变作为研究队列。评估病变的位置、形状、大小(最大直径和最大面积)和对比增强信号强度特征,并在 EN 和 HCC 病变之间进行比较。
共发现 35 例患者的 65 个 EN 病变(范围:3-60mm,平均:13.6±10.6mm)和 20 例患者的 33 个 HCC(范围:9-61mm,平均:19.3±12.6mm)。HCC 的病变形状更常为圆形或椭圆形(n=29;88%),而 EN 的病变形状更常为圆形或椭圆形(n=26;40%)(P<0.01)。出乎意料的是,一些 EN(n=12;18%)在肝细胞期呈低信号,其中 6 个(50%)T2 呈高信号。对于肝动脉期图像上小于 2cm(9 个 EN 和 21 个 HCC)的病变,肝细胞期低信号区域的平均面积(54.2±33.1mm²)明显小于相应的肝动脉期高信号区域(97.1±42.0mm²)(P=0.019),而 HCC 则没有明显差异。
EN 病变在肝细胞期偶尔可能出现低信号;呈现出诊断上的困境。在这种情况下,当肝细胞期的低信号区域小于肝动脉期的相应高血管区域时,EN 病变可与 HCC 区分开来。