Foley W D, Mallisee T A, Hohenwalter M D, Wilson C R, Quiroz F A, Taylor A J
Department of Radiology, Medical College of Wisconsin, Froedtert Memorial Lutheran Hospital, 9200 W. Wisconsin Ave., Milwaukee, WI 53226, USA.
AJR Am J Roentgenol. 2000 Sep;175(3):679-85. doi: 10.2214/ajr.175.3.1750679.
The aim of this study was to evaluate a new injection-acquisition technique performed using a multirow detector CT scanner for separation of three distinct hepatic circulatory phases (hepatic artery, portal venous inflow, hepatic venous) and to determine which of these phases is optimal for detecting hypervascular neoplasm.
Two sequential acquisitions were performed during a single breath-hold followed by a third acquisition beginning 60 sec after injection. Injection-to-scan delay for the first acquisition was the individual patient's circulation time, which was determined by a preliminary mini bolus. The mean attenuation of the upper abdominal aorta, portal vein, and hepatic parenchyma were determined for each imaging pass in 20 patients with cirrhosis and 20 patients without cirrhosis. Tumor-to-liver contrast for hypervascular primary and metastatic neoplasm was evaluated in a different set of 16 cirrhotic patients and nine noncirrhotic patients. Three-dimensional CT arteriograms were obtained from first-pass data.
Three distinct circulatory phases (hepatic artery, portal vein inflow or late arterial, and hepatic venous) were seen in cirrhotic and noncirrhotic patients. Maximum tumor-to-liver contrast for hypervascular primary and metastatic neoplasm occurred during the second pass for both cirrhotic (p < 0.006) and noncirrhotic (p < 0. 001) patients. A three-dimensional hepatic-mesenteric CT arteriogram of normal or anomalous hepatic vessels without venous overlay was obtained from first-pass data in all patients.
Rapid-sequence hepatic helical CT allows selection of the optimal time interval for hypervascular tumor detection. A new paradigm for rapid hepatic CT acquisition-namely, hepatic arterial, portal vein inflow, and hepatic venous phases-is recommended to replace hepatic artery dominant and portal venous phases.
本研究旨在评估一种使用多排探测器CT扫描仪进行的新的注射采集技术,以分离三个不同的肝循环期(肝动脉期、门静脉流入期、肝静脉期),并确定这些期中哪个对检测富血供肿瘤最为理想。
在一次屏气期间进行两次连续采集,然后在注射后60秒开始第三次采集。第一次采集的注射至扫描延迟时间为个体患者的循环时间,通过初步小剂量团注确定。测定了20例肝硬化患者和20例非肝硬化患者每次成像扫描时上腹部主动脉、门静脉和肝实质的平均衰减值。在另一组16例肝硬化患者和9例非肝硬化患者中评估了富血供原发性和转移性肿瘤的肿瘤与肝脏对比度。从首次通过的数据中获得三维CT动脉造影。
在肝硬化和非肝硬化患者中均观察到三个不同的循环期(肝动脉期、门静脉流入期或动脉晚期、肝静脉期)。对于富血供原发性和转移性肿瘤,肝硬化患者(p < 0.006)和非肝硬化患者(p < 0.001)在第二次扫描时肿瘤与肝脏对比度达到最大值。所有患者均从首次通过的数据中获得了无静脉重叠的正常或异常肝血管的三维肝肠系膜CT动脉造影。
快速序列肝脏螺旋CT可选择检测富血供肿瘤的最佳时间间隔。推荐一种新的快速肝脏CT采集模式,即肝动脉期、门静脉流入期和肝静脉期,以取代肝动脉优势期和门静脉期。