Endoscopic ultrasound elastography for evaluation of lymph nodes and pancreatic masses: A multicenter study

Marc Giovannini(Institut Paoli-Calmettes), Thomas Botelberge(Institut Paoli-Calmettes), Erwan Bories(Institut Paoli-Calmettes), Christian Pésenti(Institut Paoli-Calmettes), Fabrice Caillol(Institut Paoli-Calmettes), Benjamin Esterni(Institut Paoli-Calmettes), Geneviève Monges(Institut Paoli-Calmettes), Paolo Giorgio Arcidiacono(IRCCS Ospedale San Raffaele), Pierre H. Deprez(UCLouvain), Robert Yeung(UCLouvain), Walter Schimdt, H. Schrader, Carl Szymanski, Christoph F. Dietrich(Caritas-Krankenhaus Bad Mergentheim), Pierre Eisendrath(Université Libre de Bruxelles), Jean‐Luc Van Laethem(Université Libre de Bruxelles), Jacques Devière(Université Libre de Bruxelles), Peter Vilmann(University of Copenhagen), Adrian Săftoiu(University of Copenhagen)
World Journal of Gastroenterology
January 1, 2009
Cited by 288Open Access
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Abstract

AIM: To evaluate the ability of endoscopic ultrasound (EUS) elastography to distinguish benign from malignant pancreatic masses and lymph nodes. METHODS: A multicenter study was conducted and included 222 patients who underwent EUS examination with assessment of a pancreatic mass (n = 121) or lymph node (n = 101). The classification as benign or malignant, based on the real time elastography pattern, was compared with the classification based on the B-mode EUS images and with the final diagnosis obtained by EUS-guided fine needle aspiration (EUS-FNA) and/or by surgical pathology. An interobserver study was performed. RESULTS: The sensitivity and specificity of EUS elastography to differentiate benign from malignant pancreatic lesions are 92.3% and 80.0%, respectively, compared to 92.3% and 68.9%, respectively, for the conventional B-mode images. The sensitivity and specificity of EUS elastography to differentiate benign from malignant lymph nodes was 91.8% and 82.5%, respectively, compared to 78.6% and 50.0%, respectively, for the B-mode images. The kappa coefficient was 0.785 for the pancreatic masses and 0.657 for the lymph nodes. CONCLUSION: EUS elastography is superior compared to conventional B-mode imaging and appears to be able to distinguish benign from malignant pancreatic masses and lymph nodes with a high sensitivity, specificity and accuracy. It might be reserved as a second line examination to help characterise pancreatic masses after negative EUS-FNA and might increase the yield of EUS-FNA for lymph nodes.


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