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Characteristics and pathological mechanism on magnetic resonance diffusion-weighted imaging after chemoembolization in rabbit liver VX-2 tumor model

机译:兔肝VX-2肿瘤模型化疗栓塞后磁共振扩散加权成像的特征及病理机制

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AIM:To investigate dynamic characteristics and pathological mechanism of signal in rabbit VX-2 tumor model on diffusion-weighted imaging (DWI) after chemoembolization.rnMETHODS:Forty New Zealand rabbits were included in the study and forty-seven rabbit VX-2 tumor models were raised by implanting directly and intrahepatically after abdominal cavity opened. Forty VX-2 tumor models from them were divided into four groups. DWI was performed periodically and respectively for each group after chemoembolization. All VX-2 tumor samples of each group were studied by pathology. The distinction of VX-2 tumors on DWI was assessed by their apparent diffusion coefficient (ADC) values. The statistical significance between different time groups, different area groups or different b-value groups was calculated by using SPSS12.0 software.rnRESULTS:Under b-value of 100 s/mm~2, ADC values were lowest at 16 h after chemoembolization in area of VX-2 tumor periphery, central, and normal liver parenchyma around tumor, but turned to increase with further elongation of chemoembolization treatment. The distinction of ADC between different time groups was significant respectively (F = 7.325, P < 0.001; F = 2.496, P < 0.048; F = 6.856, P < 0.001). Cellular edemarnin the area of VX-2 tumor periphery or normal liver parenchyma around tumor, increased quickly in sixteen h after chemoembolization but, from the 16th h to the 48th h, cellular edema in the area of normal liver parenchyma around tumor decreased gradually and that in the area of VX-2 tumor periphery decreased lightly at, and then increased continually. After chemoembolization, Cellular necrosis in the area of VX-2 tumor periphery was more significantly high than that before chemoembolization. The areas of dead cells in VX-2 tumors manifested low signal and high ADC value, while the areas of viable cells manifested high signal and low ADC value.rnCONCLUSION:DWI is able to detect and differentiate tumor necrotic areas from viable cellular areas before and after chemoembolization. ADC of normal liver parenchyma and VX-2 tumor are influenced by intracellular edema, tissue cellular death and microcirculation disturbance after chemoembolization.
机译:目的:探讨化学栓塞后弥散加权成像(DWI)在兔VX-2肿瘤模型中信号的动态特征和病理机制。方法:研究对象:新西兰大白兔40只,兔VX-2肿瘤模型47只腹腔开放后直接和肝内植入来种植牙。将其中的40种VX-2肿瘤模型分为四组。化疗栓塞后,每组定期进行DWI。通过病理学研究每组的所有VX-2肿瘤样品。 VX-2肿瘤在DWI上的区别通过其表观扩散系数(ADC)值进行评估。应用SPSS12.0软件计算不同时间组,不同区域组或不同b值组之间的统计学显着性。结果:在100 s / mm〜2的b值下,化学栓塞后16 h ADC值最低。 VX-2肿瘤在肿瘤周围,中心和正常肝实质的面积,但随着化学栓塞治疗的进一步延长而增加。 ADC在不同时间组之间的区别分别很明显(F = 7.325,P <0.001; F = 2.496,P <0.048; F = 6.856,P <0.001)。在化学栓塞后的16小时内,肿瘤周围的VX-2肿瘤周围或正常肝实质中的细胞edemarnin迅速增加,但从第16 h至第48 h,肿瘤周围正常肝实质中的细胞水肿逐渐减少,并且VX-2肿瘤周围区域的γ在处轻微降低,然后持续增加。化学栓塞后,VX-2肿瘤周围区域的细胞坏死比化学栓塞前更高。 VX-2肿瘤中的死细胞区域显示低信号和高ADC值,而活细胞区域显示高信号和低ADC值。rn结论:DWI能够在之前和之后从活细胞区域检测和区分肿瘤坏死区域化学栓塞后。正常肝实质和VX-2肿瘤的ADC受化学栓塞后细胞内水肿,组织细胞死亡和微循环障碍的影响。

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