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作 者:胡玉川[1] 孟菲[2] 张贝[1] 李刚锋[1] 于瀛[1] 崔光彬[1]
机构地区:[1]第四军医大学唐都医院放射科,西安710038 [2]武警黑龙江省总队医院放射科,哈尔滨150076
出 处:《放射学实践》2014年第4期404-407,共4页Radiologic Practice
摘 要:目的:探讨胸腺上皮性肿瘤(TETs)的WHO病理分型与CT表现的相关性,以提高其CT诊断及临床诊疗水平。方法:回顾性分析经穿刺活检或手术病理证实的66例TETs患者的CT影像学表现。所有患者均行胸部CT平扫及增强扫描,均经组织病理学及细胞免疫组化检查并进行WHO组织病理分型,分析TETs各种组织学类型的CT特征。结果:66例TETs中男39例,女27例,年龄6~77岁。病理分型:A型5例(7.6%),AB型15例(22.7%),B1型13例(19.7%),B2型10例(15.2%),B3型10例(15.2%)及胸腺癌13例(19.7%)。A、AB、B1型胸腺瘤均呈圆形或类圆形,而80.0%的B3型胸腺瘤及92.3%的胸腺癌呈不规则形;大部分(92.4%)胸腺肿瘤呈中度强化。80.0%B3型胸腺瘤及100%胸腺癌有包膜破坏并侵犯邻近结构;40.0%的B3型胸腺瘤及61.5%的胸腺癌出现心包和(或)胸膜腔积液;随着肿瘤病理分级的增加,周围结构受侵的发生率亦随之升高,分别为15.4%(B1)、40.0%(B2)、80.0%(B3)及100%(胸腺癌)。TETs组织学分类与侵袭危险度CT分级之间存在显著相关性(rs=0.736,P〈0.01)。结论:不同WHO病理分型的TETs的cT表现具有一定特征性,TETs的CT特征反映了其侵袭危险性及组织病理学分型。Objective:To study the relationship between WHO pathology subtypes and CT features of thymic epithelial tumors (TETs) for improving the diagnostic accuracy of CT. Methods: The plain and enhanced CT findings of 66 pa tients with TETs confirmed by pathology (needle biopsy/surgery and pathology) with WHO classification and histo-immunohistochemistry were retrospectively analyzed. The CT findings were correlated with pathology subtypes. Results:Of the 66 patients with TETs,there were 39 men and 27 women; the age ranged from 6 - 77y. The WHO pathology subtypes were: Type A (n=5,7.6%) ;Type AB (n= 15,22.7%) ;Type B1 (n=13,19.7%) ;Type B2 (n=10,15.2%);Type B3 (n=10, 15.2 % ) ;and thymic carcinoma (n= 13,19.7 % ). The shape of Type A, Type AB and Type B1 tumors were mostly round or oval,whereas 80.0% of Type B3 tumors and 92.3% of thymic carcinomas were irregular in shape. There was a moderate enhancement after contrast injection in most of the thymomas (92.4 % ). Capsule destruction or invasion to the adjacent tissue occurred in 80.0% of Type B3 thymomas and 100% of thymic carcinomas,respectively. Pleural and/or pericardial effu sion occurred in 40.0% of Type B3 thymomas and 61.5% of thymic carcinomas, respectively. As the upgrading of malig- nancy degree of pathology, the incidence of adjacent structures invasion increased, which was: 15.4 % (Type B1), 40.0 % (Type B2),80.0% (Type B3) and 100% (thymic carcinomas), respectively. There was a significant correlation between WHO pathology subtypes of TETs and the risk of aggressiveness graded by CT (rs= O. 736, P〈0.01). Conclusion:Diffe rent WHO pathology subtypes of TET had their CT characteristics varied. CT features of TETs might reflect their pathology subtypes and aggressiveness.
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