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Evaluation of malignant breast lesions in the diagnostic setting with cone beam breast computed tomography (Breast CT): Feasibility study

机译:锥形束乳腺计算机断层摄影术(乳腺CT)在诊断环境中评估乳腺恶性病变的可行性研究

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To investigate the feasibility of noncontrast and contrast-enhanced cone beam breast Computed Tomography (CT) in demonstrating malignant breast lesions in the diagnostic setting. This Institutional Review Board approved, Health Information Portability and Accountability Act compliant, prospective study enrolled BI-RADS four and five patients from 2008 to 2010. Eighty-seven subjects had noncontrast breast CT, 42 had contrast-enhanced breast CT (CE-breast CT) with 70 pathologically confirmed cancer diagnoses. All 70 comprise the study cohort for noncontrast breast CT, and 23 who had CE-breast CT comprise the cohort for CE-breast CT. All had diagnostic work-up. Patient age, breast density, lesion size and characteristics, biopsy method, and core pathology were recorded. A Fisher's exact test was used to detect a difference in detectability. For agreement in size measurement between the imaging modalities, a paired t-test was employed. Reported p-values were based on 2-sided tests. Two one-sided tests were calculated to determine equivalence within ±0.3 cm at a 90% significance level. Noncontrast breast CT identified 67 of 70 malignant lesions, detected by diagnostic work-up. CE-breast CT identified 23 of 23 index malignant lesions and in addition, found three malignant lesions in three cases not previously detected. Noncontrast breast CT demonstrated the index lesion in 67 of 70 cases and CE-breast CT demonstrated the index lesion in all 23 cases. An additional three new malignant lesions not seen with conventional diagnostic work-up were detected. In this preliminary study, breast CT with or without contrast was shown to be accurate at identifying malignant breast lesions in the diagnostic setting.
机译:目的探讨无反差和增强对比锥束乳腺计算机断层扫描(CT)在诊断环境中证明乳腺恶性病变的可行性。经机构审查委员会批准,符合《健康信息携带和责任法案》的前瞻性研究从2008年至2010年招募了BI-RADS的4例和5例患者。87例患者进行了CT造影,而42例进行了对比增强的乳腺CT(CE乳腺CT) )具有70个经过病理证实的癌症诊断。所有70例均属于非对比乳腺CT的研究队列,而23例具有CE乳腺CT的人群构成了CE乳腺CT队列。全部进行了诊断检查。记录患者年龄,乳房密度,病变大小和特征,活检方法以及核心病理。 Fisher精确检验用于检测可检测性的差异。为了使成像模态之间的尺寸测量一致,采用了配对t检验。报告的p值基于2面检验。计算了两个单面测试,以90%的显着性水平确定±0.3 cm以内的当量。非对比乳腺CT通过诊断检查发现了70个恶性病变中的67个。 CE-乳腺CT识别了23个指标性恶性病变中的23个,此外,在3例先前未发现的病例中发现了3个恶性病变。非对比乳腺CT显示70例中有67例有病变,CE-乳腺CT显示23例中有病变。在常规诊断检查中未发现另外三个新的恶性病变。在这项初步研究中,无论有无对比,乳腺CT在诊断环境中均能准确识别乳腺恶性病变。

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