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Solid pancreatic lesions: The choice of fine-needle aspiration-needle to optimize the diagnosis

INTRODUCTION: Endoscopic ultrasonography (EUS)-guided fine-needle aspiration (FNA) have a better accuracy for the detection of pancreatic tumors compared with others images modalities. We assessed if the image criteria of elastography and contrast harmonic echo-endoscopic ultrasound could help in ch...

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Autores principales: Francioni, E., Reimão, S., Bories, E., Caillol, F., Pesenti, C., Poizat, F., Monges, G., Giovannini, M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4569908/
https://www.ncbi.nlm.nih.gov/pubmed/26425510
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author Francioni, E.
Reimão, S.
Bories, E.
Caillol, F.
Pesenti, C.
Poizat, F.
Monges, G.
Giovannini, M.
author_facet Francioni, E.
Reimão, S.
Bories, E.
Caillol, F.
Pesenti, C.
Poizat, F.
Monges, G.
Giovannini, M.
author_sort Francioni, E.
collection PubMed
description INTRODUCTION: Endoscopic ultrasonography (EUS)-guided fine-needle aspiration (FNA) have a better accuracy for the detection of pancreatic tumors compared with others images modalities. We assessed if the image criteria of elastography and contrast harmonic echo-endoscopic ultrasound could help in choosing the appropriate FNA-needle in the evaluation of focal pancreatic mass in other to maximize the diagnostic yield. This study prospectively included all new patients with focal pancreatic masses referred to be examined by EUS from October to December/2013. A total of 21 patients performed EUS with sequentially elastography and intravenous injection of a second-generation contrast agent (2.4 mL of SonoVue, Braco International, The Netherlands). The lesions which appear hipovascular were assessed with 22 gauge or 25 gauge FNA-needles. The hipervascular masses were biopsied with 19 gauge needles. RESULTS: The topography of the lesions varied on 13 at the head, 4 at the body and 1 on the tail. The finding of a hypoenhanced mass was found in 57% (12/21 patients). Hyperenhanced was detected in 28% (6/21 patients). There were 14% (three patients) which the data were not recorded. The cytological diagnosis was achieved in 81% (17/21 patients) on the first biopsy. The others four patients have reached the diagnosis on the second examination. Of those four patients, in one was used the ProCore 25 gauge (lesion on the uncinatus process), and another one was used both 22 gauge and 25 gauge in the first examination. CONCLUSION: A characterization of the pancreatic lesions with elastography and contrast agents might be useful for clinical decision of which needle is better to improve biopsy quality and minimize EUS-FNA negatives results.
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spelling pubmed-45699082015-09-30 Solid pancreatic lesions: The choice of fine-needle aspiration-needle to optimize the diagnosis Francioni, E. Reimão, S. Bories, E. Caillol, F. Pesenti, C. Poizat, F. Monges, G. Giovannini, M. Endosc Ultrasound EURO EUS Meeting INTRODUCTION: Endoscopic ultrasonography (EUS)-guided fine-needle aspiration (FNA) have a better accuracy for the detection of pancreatic tumors compared with others images modalities. We assessed if the image criteria of elastography and contrast harmonic echo-endoscopic ultrasound could help in choosing the appropriate FNA-needle in the evaluation of focal pancreatic mass in other to maximize the diagnostic yield. This study prospectively included all new patients with focal pancreatic masses referred to be examined by EUS from October to December/2013. A total of 21 patients performed EUS with sequentially elastography and intravenous injection of a second-generation contrast agent (2.4 mL of SonoVue, Braco International, The Netherlands). The lesions which appear hipovascular were assessed with 22 gauge or 25 gauge FNA-needles. The hipervascular masses were biopsied with 19 gauge needles. RESULTS: The topography of the lesions varied on 13 at the head, 4 at the body and 1 on the tail. The finding of a hypoenhanced mass was found in 57% (12/21 patients). Hyperenhanced was detected in 28% (6/21 patients). There were 14% (three patients) which the data were not recorded. The cytological diagnosis was achieved in 81% (17/21 patients) on the first biopsy. The others four patients have reached the diagnosis on the second examination. Of those four patients, in one was used the ProCore 25 gauge (lesion on the uncinatus process), and another one was used both 22 gauge and 25 gauge in the first examination. CONCLUSION: A characterization of the pancreatic lesions with elastography and contrast agents might be useful for clinical decision of which needle is better to improve biopsy quality and minimize EUS-FNA negatives results. Medknow Publications & Media Pvt Ltd 2014-04 /pmc/articles/PMC4569908/ /pubmed/26425510 Text en Copyright: © Endoscopic Ultrasound http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle EURO EUS Meeting
Francioni, E.
Reimão, S.
Bories, E.
Caillol, F.
Pesenti, C.
Poizat, F.
Monges, G.
Giovannini, M.
Solid pancreatic lesions: The choice of fine-needle aspiration-needle to optimize the diagnosis
title Solid pancreatic lesions: The choice of fine-needle aspiration-needle to optimize the diagnosis
title_full Solid pancreatic lesions: The choice of fine-needle aspiration-needle to optimize the diagnosis
title_fullStr Solid pancreatic lesions: The choice of fine-needle aspiration-needle to optimize the diagnosis
title_full_unstemmed Solid pancreatic lesions: The choice of fine-needle aspiration-needle to optimize the diagnosis
title_short Solid pancreatic lesions: The choice of fine-needle aspiration-needle to optimize the diagnosis
title_sort solid pancreatic lesions: the choice of fine-needle aspiration-needle to optimize the diagnosis
topic EURO EUS Meeting
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4569908/
https://www.ncbi.nlm.nih.gov/pubmed/26425510
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