首页> 外文OA文献 >Core Needle Biopsy Targeting the Viable Area of Deep-Sited Dominant Lesion Verified by Color Doppler and/or Contrast-Enhanced Ultrasound Contribute to the Actionable Diagnosis of the Patients Suspicious of Lymphoma
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Core Needle Biopsy Targeting the Viable Area of Deep-Sited Dominant Lesion Verified by Color Doppler and/or Contrast-Enhanced Ultrasound Contribute to the Actionable Diagnosis of the Patients Suspicious of Lymphoma

机译:核心针活检靶向彩色多普勒和/或对比增强超声验证的深针型显性病变的可行性区域有助于可操作的患者可操作的淋巴瘤的诊断

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摘要

BackgroundInadequate accuracy of ultrasound-guided core needle biopsy (US-CNB) urges further improvement for the diagnosis and management of lymphoma to meet with the practitioners’ increased reliance on this mini-invasive approach.MethodsData related to US-CNB of the deep-sited dominant lesions suspicious of lymphoma detected by computer tomography or positron-emission tomography/computer tomography for eligibility assessment of three prospective clinical trials were collected in advance. A retrospective analysis of the prospective data collection was performed, in which Viable-targeting US-CNB that Color Doppler flow imaging (CDFI) and/or contrast enhanced ultrasound (CEUS) were employed to select viable area for biopsy target compared with Routine US-CNB that routine procedure of evaluation and guidance using gray-scale ultrasound with CDFI in terms of the yield of clinically actionable diagnosis and safety, and determinants for the successful US-CNB that established an actionable diagnosis were explored. The establishment of final diagnosis was based on surgical pathology or medical response to therapy with follow-up at least 6 months.ResultsA total of 245 patients underwent Routine US-CNB (N = 120) or Viable-targeting US-CNB (N = 125), of which 91 (91/120, 75.8%) and 112 (112/125, 89.6%) were revealed with actionable diagnoses, respectively (p = 0.004, OR 0.846, 95% CI: 0.753–0.952). And 239 patients established final diagnoses. Diagnostic yields of actionable diagnosis according to the final diagnoses were 78.4% (91/116) and 91.1% (112/123) (p = 0.006, OR 0.554, 95% CI: 0.333–0.920), 82.6% (90/109) and 92.5% (111/120) for malignancy, 84.0% (84/100) and 91.8% (101/110) for lymphoma, 85.1% (80/94) and 92.3% (96/104) for Non-Hodgkin Lymphoma, 66.7% (4/6) and 83.3% (5/6) for Hodgkin Lymphoma in Routine and Viable-targeting CNB groups, respectively. No major complications were observed. Dominant lesions with actionable diagnosis in US-CNB were with higher FDG-avid Standardized Uptake Value. Binomial logistic regression revealed that actionable diagnosis of US-CNB was correlated with group and ancillary studies.ConclusionViable-Targeting US-CNB was superior to routine US-CNB in term of the yield of actionable diagnosis for deep-sited dominant lesions suspicious of lymphoma, which demonstrated a potential to be the initial approach in this setting.
机译:背景技术超声引导芯针活检(US-CNB)促进淋巴瘤的诊断和管理进一步改善,以与从业者的依赖于这种迷你侵略性方法的依赖..关于我们-CNB的深度突出的提前收集计算机断层扫描或正电子释放断层扫描/计算机断层扫描的淋巴瘤的主导病变被提前收集三个前瞻性临床试验的资格评估。对前瞻性数据收集的回顾性分析,其中使用彩色多普勒流量成像(CDFI)和/或对比增强超声(CEUS)的可行靶向US-CNB,与常规US-相比为活组织检查靶标选择可行的区域。 CNB认为,在临床上可操作的诊断和安全的产量方面,使用CDFI使用CDFI进行评估和指导的常规程序,以及建立可操作诊断的成功US-CNB的决定因素。最后诊断的建立是基于外科病理学或治疗医学反应与后续的至少6 months.ResultsA总的245例患者进行常规US-CNB(N = 120)或存活的靶向US-CNB(N = 125 ),其中91(91/120,75.8%)和112(112/125,89.6%)分别揭示了可操作的诊断(p = 0.004,或0.846,95%Ci:0.753-0.952)。和239名患者建立了最终诊断。根据最终诊断的可操作诊断的诊断产量为78.4%(91/116)和91.1%(112/123)(p = 0.006,或0.554,95%Ci:0.333-0.920),82.6%(90/109)对于恶性肿瘤,84.0%(84/100)和91.8%(101/110)的92.5%(111/120),淋巴瘤85.1%(80/94)和92.3%(96/104)用于非霍奇金淋巴瘤, 66.7%(4/6)和83.3%(5/6)分别用于常规和可行靶向CNB组的核糖淋巴瘤。没有观察到主要并发症。 US-CNB中具有可操作诊断的显性病变具有更高的FDG-Avid标准化摄取值。二项式逻辑回归揭示了US-CNB的可操作诊断与组和辅助研究相关。可操作靶向US-CNB的常规US-CNB在淋巴瘤的可操作诊断的可操作诊断的率方面优于常规US-CNB,这表明了这种设置中的初始方法。

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