检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:孟洁[1] 张凤娟[1] 周军华[1] 赵娜[1] 韩若凌[1]
机构地区:[1]河北医科大学第四医院超声科,石家庄市050011
出 处:《中国超声医学杂志》2012年第11期1006-1008,共3页Chinese Journal of Ultrasound in Medicine
基 金:河北省卫生厅医学科学研究重点课题计划(No.20100417);河北省高校强势特色学科第四医院肿瘤学支持项目(冀教高No.[2005]52)
摘 要:目的探讨声触诊组织量化技术对脂肪肝内低回声病变的定性诊断价值。方法应用常规超声与声触诊组织量化技术对106个脂肪肝内低回声病变进行检查,对检查结果进行对比分析,鉴别诊断其良、恶性。结果肝细胞性肝癌、肝转移癌及肝良性病变剪切波速分别为(2.31±1.09)、(2.42±1.18)、(1.35±0.87)m/s,肝细胞性肝癌、肝转移癌组与肝良性病变组剪切波速比较差异均有统计学意义(P<0.05),肝细胞性肝癌与肝转移癌剪切波速比较差异无统计学意义(P>0.05)。脂肪肝内的低回声病变常规超声鉴别恶性病变的敏感度、特异度、准确率分别为45.45%(20/44)、75.61%(62/82)、67.92%(72/106),以2 m/s作为恶性病变的诊断标准,声触诊组织量化技术鉴别恶性病变的敏感度、特异度、准确率分别为95.45%(42/44)、96.87%(62/64)、96.36%(102/106)。结论声触诊组织量化技术可显著提高脂肪肝内低回声病变的定性诊断效能。Objective To investigate qualitative value of virtual tough tissues quantification (VTQ) of focal hy poechoic lesions in fatty liver. Methods Totally 106 lesions in fatty liver in 86 patients were examined using both con ventional sonography and VTQ. Results There was significant difference of share wave velocity between malignant group and benign group(P〈0.05). There was no significant difference of share wave velocity between primary hepatic malignant tumors and metastatic liver tumors(P〉0.05). For the discrimination of malignant versus benign hypoechoic lesions in fatty livers, receiver operating characteristic analysis revealed a significant improvement in this discrimina tion. For the discrimination of malignant versus benign liver lesions, with a cut-off value of 2 m/s for share wave ve locity, VTQ improved sensitivity from 45.45% to 95.45%, specificity from 75.61% to 96.87% and accuracy from 67.92% to 96.36 % compared with conventional sonography. Conclusions With VTQ,characterization and diagnostic performance of hypoechoic liver lesions in fatty liver are greatly improved.
关 键 词:声触诊组织量化技术脂肪肝低回声 鉴别诊断
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:18.191.138.59