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作 者:于春英[1,2] 颜林枫[1] 刘志成[1] 韩宇[1] 胡玉川[1] 李刚锋[1] 于 瀛[1] 孙倩[1] 王文[1] 崔光彬[1]
机构地区:[1]第四军医大学唐都医院放射科,陕西西安710038 [2]西安医学院第一附属医院影像科
出 处:《实用放射学杂志》2016年第6期829-832,共4页Journal of Practical Radiology
基 金:陕西省社发攻关课题(2012K13-02-27).
摘 要:目的 评价3D-FSE Cube序列对垂体微腺瘤的诊断价值。方法 对47例垂体微腺瘤的2D-FSE、3D-FSE Cube序列图像进行评分,评价指标如下:①病变与正常垂体的分界;②正常垂体与海绵窦分界;③垂体柄显示;④总体图像质量;⑤磁化率伪影。并计算2组检出率。图像评分应用Wilcoxon符号秩检验。评价者间一致性采用Kappa值表示。P<0.05有统计学意义。结果3D-FSE Cube序列在图像质量方面优于2D-FSE序列(P<0.05),T1WI的磁化率伪影明显比2D-FSE序列少(P<0.01)。3D-FSE Cube、2D-FSE序列对垂体微腺瘤的总检出率分别为100%(47/47)、85.1%(40/47),其中T1WI的检出率分别为97.9%(46/47)、57.4%(27/47)。评价者间一致性较高,T1WI、T2WI的k值分别为0.86、0.88。结论3D-FSE Cube序列显示垂体微腺瘤明显优于2D-FSE序列,扫描时间缩短20~27 s,具有重要的临床应用价值。Objective To assess the value of 3D-FSE Cube sequence in diagnosis of pituitary micro-adenoma. Methods 3D-FSE Cube as well as 2D-FSE images of the pituitary were acquired in 47 patients with known pituitary micro-adenoma. Two experienced radiologists evaluated the images quality by the following criteria: ①the border between the pituitary gland and the lesion ; ②boundary edge of the cavernous sinus and pituitary gland; ③visualization of the pituitary stalk; ④overall image quality; ⑤ susceptibility artifacts. The detection rates in two groups were calculated and analyzed statistically. Qualitative analyses were accomplished by Wilcoxon signed-rank test. The interobserver agreement assessment was analyzed with K-statistics. P〈0.05 was considered to have a statistically significant difference. Results The image quality of 3D-FSE Cube sequence is better than that of 2D-FSE sequence (P〈0. 05), and T1-weighted imaging (T1N I) showed fewer susceptibility artifacts in 3D-FSE Cube sequence (P〈0. 01). The detection rates of 3D-FSE Cube and 2D-FSE were 100% (47/47), 85.1% (40/47), respectively, of which on T1WI were 97.9% (46/47), 57.4% (27/47). The results of the two observers were in a great agreement on T1WI (k=0.86) and T2WI (k=0.88). Conclusion 3D-FSE Cube sequence with superior image quality,of which the scan time decreased about 20-27 s, is proved to be an available clinical detection of pituitary micro-adenoma.
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