Yield of Contrast-Enhanced Power Doppler Endoscopic Ultrasonography and Strain Ratio Obtained by EUS-Elastography in the Diagnosis of Focal Pancreatic Solid Lesions.

Yield of Contrast-Enhanced Power Doppler Endoscopic Ultrasonography and Strain Ratio Obtained by EUS-Elastography in the Diagnosis of Focal Pancreatic Solid Lesions.
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DOI:
10.7178/eus.03.005
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发表时间:
2012-10
影响因子:
4.5
通讯作者:
Giovannini M
Giovannini M
中科院分区:
医学1区
文献类型:
--
作者:
Figueiredo FA;da Silva PM;Monges G;Bories E;Pesenti C;Caillol F;Delpero JR;Giovannini M

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虽然内镜超声引导下细针穿刺(EUS-FNA)是诊断胰腺病变的金标准,但其阴性预测值并不理想。我们的目的是评价对比增强EUS(CED-EUS)和应变比EUS弹性成像(SR-E-EUS)鉴别胰腺实性病变的能力。47例患者(27例男性,20例女性,70 ± 11岁)连续参与了这项单中心前瞻性研究。将其提交给EUS、SR-E-EUS、CED-EUS(使用Sonovue®)和EUS-FNA。最终诊断基于EUS-FNA和/或手术标本(如可用)的组织学评估以及至少6个月的随访。47例胰腺局灶性病变中,良性病变13例(28%),恶性病变34例(72%)。恶性肿瘤患者年龄较大(70 ± 11 vs. 61 ± 8,P = 0.003),病变较大(34 ± 12 mm vs. 22 ± 11 mm,P = 0.03)。恶性病变SR-E-EUS高(31 ± 32 vs. 8 ± 9,P = 0.001),低血供型多(93% vs. 33%,P < 0.001)。Logistic回归分析表明,只有低血供(OR = 2.6,95%CI:1.5-130,P = 0.02)是恶性肿瘤的独立预测因素。SR-E-EUS的ROC分析得出恶性肿瘤最佳功效区分的最佳截止值为8(AUC 0.91,95%CI:0.74-0.98)。EUS-FNA、SR-E-EUS和CED-EUS的敏感性(79%、90%、93%)和特异性(85%、75%、67%)无显著差异。通过对不确定的EUS-FNA亚组(9例患者,19%)的分析,SR-E-EUS > 8和血供减少的敏感性分别为80%和100%,特异性分别为67%和67%。CED-EUS和SR-E-EUS的临床实用性仍存在疑问。CED-EUS和SR-E-EUS的准确性与EUS-FNA相似。血供不足是恶性肿瘤的独立预测指标。EUS-FNA不确定的患者可以受益于CED-EUS,因为血管减少诊断恶性肿瘤的敏感性高。
Although endoscopic ultrasonography-guided fine needle aspiration (EUS-FNA) is the gold standard for diagnosing pancreatic lesions, its negative predictive value is suboptimal. Our aim was to evaluate the yield of contrast-enhanced EUS (CED-EUS) and of strain ratio EUS-elastography (SR-E-EUS) for differentiating pancreatic solid lesions. Forty-seven patients (27 men, 20 women, 70 ± 11 years) were consecutively involved in this single-center, prospective study. They were submitted to EUS, SR-E-EUS, CED-EUS with Sonovue®, and EUS-FNA. The final diagnosis was based on the histological assessment of EUS-FNA and/or surgical specimens when available, and on follow-up of at least 6 months. From the 47 focal pancreatic lesions included, 13 (28%) were benign and 34 (72%) malignant. Patients with malignancy were older (70 ± 11 vs. 61 ± 8, P = 0.003), and had larger lesions (34 ± 12 mm vs. 22 ± 11 mm, P = 0.03). Malignant lesions had higher SR-E-EUS (31 ± 32 vs. 8 ± 9, P = 0.001) and more hypovascular pattern (93% vs. 33%, P < 0.001). Logistic regression determined that only hypovascularity (OR = 2.6, 95%CI: 1.5-130, P = 0.02) was independently predictive of malignancy. ROC analysis for SR-E-EUS yielded an optimal cutoff of 8 (AUC 0.91, 95%CI: 0.74-0.98) for the best power distinction for malignancy. There was no significant difference concerning sensitivity (79%, 90%, 93%) and specificity rates (85%, 75%, 67%) of EUS-FNA, SR-E-EUS, and CED-EUS, respectively. By analysis of the inconclusive EUS-FNA subset (9 patients, 19%), SR-E-EUS > 8 and hypovascularity showed sensitivity of 80% and 100%, and specificity of 67% and 67%, respectively. The clinical utility of CED-EUS and SR-E-EUS remains questionable. The accuracies of CED-EUS and SR-E-EUS are similar to EUS-FNA. Hypovascularity was independently predictive of malignancy. Patients with inconclusive EUS-FNA could benefit from CED-EUS due to the high sensitivity of hypovascularity for diagnosing malignancy.
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