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作 者:管逊 庄治国[1] 池嘉昌[1] 王文晶[1] 王嵇[1] 周炜[1] 许建荣[1]
机构地区:[1]上海交通大学医学院附属仁济医院放射科,上海200127
出 处:《生物医学工程与临床》2014年第3期236-241,共6页Biomedical Engineering and Clinical Medicine
基 金:国家自然科学基金资助项目(81201172)
摘 要:目的探讨运用平板探测器CT灌注成像(FD—CTP)在肝细胞癌(HCC)中评估血容量(BV)的可行性,并与传统CT灌注成像(CTP)进行比较。方法选择20例HCC患者,其中男性13例,女性7例;年龄36—82岁,中位年龄58岁。先后进行传统CTP检查和FD—CTP检查,首先运用CTP测量肿瘤和肝实质区BV值(CTP—BV),再运用FD—CTP测量相对应区的BV值(FD—BV),根据下列等式提取CTP-BV中的动脉灌注产生部分(CTP—BVarterial):CTP—BVarterial=CTP—BV×HPI(HPI为肝动脉灌注指数)。另外假设:肝肿瘤的CTP-BVarterial/肝实质的CTP-BVarterial=CTP-BVarterial相对值,肝肿瘤的FD—BV/肝实质的FD—BV=FD—BV相对值。分析两种检查BV值的关系。结果CTP-BVarterial和FD—BV绝对值之间有良好的相关性(HCC:r=0.903:肝实质:r=0.920;P〈0.001)。B1and—Altman检验显示,CTP—BVarterial和FD—BV相对值的平均差值为-0.15±0.24。结论HCC或肝实质的FD-BV和CTP-BVarterial值均具有良好的可比性,肝脏FD—CTP检查在临床上具有可行性。Objective To investigate the feasibility of determining blood volume(BV) in hepatoeellular carcinoma(HCC) by using flat detector computed tomography perfusion (FD-CTP), and compare the measurements between FD-CTP and conventional CT perfusion(CTP). Methods A total of 20 HCC patients enrolled, included 13 males and 7 females, aged 36 - 82 year old with median age of 58. All of them were given CTP, and then FD-CTP was performed. The BV values of CTP (CTP-BV) and FD-CTP(FD-BV) were measured within tumors and liver parenehyma correspondingly. The arterial perfusion portion of CTP -BV (CTP-BVarterial) was extracted under the assumption of CTP-BVarterial = CTP-BVarterial HPI(HPh represents hepatic perfusion index). Relative value(RV) for CTP-BVarterial was defined as CTP-BVarterial of tumor / CTP-BVarterial of parenchyma, and RV for FD-BV was defined as FD-BV of tumor / FD-BV of parenehyma. Relationships between BV values of 2 techniques were analyzed. Results There were good correlations between the absolute values of FD-BV and CTP-BVarterial (tumor r = 0.903, parenchyma r = 0.920, both P 〈 0.001). Bland-Ahman analysis showed mean difference of - 0.15 ± 0.24 between RV for CTP-BVarterial and FD-BV. Conclusion It is demonstrated that FD-BV have good comparability with CTP-BVarterial in both HCC and liver parenchyma, and FD-CTP for liver seems to be feasible in clinical use.
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