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Pancreatic cystic lesions: The value of contrast-enhanced endoscopic ultrasound to influence the clinical pathway
BACKGROUND AND OBJECTIVES: Cystic pancreatic lesions are a growing diagnostic challenge. The aim of this study was to proof a new diagnostic concept based on contrast-enhanced endoscopic ultrasound (CE-EUS) for differential diagnosis. PATIENTS AND METHODS: A total of 125 patients with unclear cystic...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4064160/ https://www.ncbi.nlm.nih.gov/pubmed/24955342 http://dx.doi.org/10.4103/2303-9027.131040 |
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author | Hocke, Michael Cui, Xin-Wu Domagk, Dirk Ignee, Andre Dietrich, Christoph F. |
author_facet | Hocke, Michael Cui, Xin-Wu Domagk, Dirk Ignee, Andre Dietrich, Christoph F. |
author_sort | Hocke, Michael |
collection | PubMed |
description | BACKGROUND AND OBJECTIVES: Cystic pancreatic lesions are a growing diagnostic challenge. The aim of this study was to proof a new diagnostic concept based on contrast-enhanced endoscopic ultrasound (CE-EUS) for differential diagnosis. PATIENTS AND METHODS: A total of 125 patients with unclear cystic pancreatic lesions were included. The initial diagnostic was made by CE-EUS dividing the lesions in a group without contrast enhancing effect in the cystic wall, septae or nodule indicating pseudocysts or dysontogenetic cysts and a group with contrast enhancing effect in the described structures indicating cystic neoplasias. The investigations were performed using a Pentax echoendoscope and Hitachi Preirus ultrasound machine. The contrast enhancer used was 4.8 mL SonoVue(®) (Bracco, Italy). The group with suspected cystic neoplasia was referred for endoscopic fine-needle puncture for further diagnostic or treatment decisions. RESULTS: The dividing of the groups by contrast-enhanced ultrasound was feasible because all (n = 56) suspected cystic neoplasias showed a contrast enhancing effect, whereas in only 4 from 69 pseudocystic or dysontogenetic cystic lesions a contrast enhancing effect in the wall could be observed. Endoscopic fine-needle puncture could diagnose all malignant neoplasias and relevant premalignant conditions. The long-term follow-up did not show any development of malignant cystic lesions. CONCLUSION: Using CE-EUS and endoscopic fine-needle puncture as diagnostic criteria seemed to be a feasible method to deal with different cystic lesions in daily practice. |
format | Online Article Text |
id | pubmed-4064160 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-40641602014-06-20 Pancreatic cystic lesions: The value of contrast-enhanced endoscopic ultrasound to influence the clinical pathway Hocke, Michael Cui, Xin-Wu Domagk, Dirk Ignee, Andre Dietrich, Christoph F. Endosc Ultrasound Original Article BACKGROUND AND OBJECTIVES: Cystic pancreatic lesions are a growing diagnostic challenge. The aim of this study was to proof a new diagnostic concept based on contrast-enhanced endoscopic ultrasound (CE-EUS) for differential diagnosis. PATIENTS AND METHODS: A total of 125 patients with unclear cystic pancreatic lesions were included. The initial diagnostic was made by CE-EUS dividing the lesions in a group without contrast enhancing effect in the cystic wall, septae or nodule indicating pseudocysts or dysontogenetic cysts and a group with contrast enhancing effect in the described structures indicating cystic neoplasias. The investigations were performed using a Pentax echoendoscope and Hitachi Preirus ultrasound machine. The contrast enhancer used was 4.8 mL SonoVue(®) (Bracco, Italy). The group with suspected cystic neoplasia was referred for endoscopic fine-needle puncture for further diagnostic or treatment decisions. RESULTS: The dividing of the groups by contrast-enhanced ultrasound was feasible because all (n = 56) suspected cystic neoplasias showed a contrast enhancing effect, whereas in only 4 from 69 pseudocystic or dysontogenetic cystic lesions a contrast enhancing effect in the wall could be observed. Endoscopic fine-needle puncture could diagnose all malignant neoplasias and relevant premalignant conditions. The long-term follow-up did not show any development of malignant cystic lesions. CONCLUSION: Using CE-EUS and endoscopic fine-needle puncture as diagnostic criteria seemed to be a feasible method to deal with different cystic lesions in daily practice. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC4064160/ /pubmed/24955342 http://dx.doi.org/10.4103/2303-9027.131040 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 | Original Article Hocke, Michael Cui, Xin-Wu Domagk, Dirk Ignee, Andre Dietrich, Christoph F. Pancreatic cystic lesions: The value of contrast-enhanced endoscopic ultrasound to influence the clinical pathway |
title | Pancreatic cystic lesions: The value of contrast-enhanced endoscopic ultrasound to influence the clinical pathway |
title_full | Pancreatic cystic lesions: The value of contrast-enhanced endoscopic ultrasound to influence the clinical pathway |
title_fullStr | Pancreatic cystic lesions: The value of contrast-enhanced endoscopic ultrasound to influence the clinical pathway |
title_full_unstemmed | Pancreatic cystic lesions: The value of contrast-enhanced endoscopic ultrasound to influence the clinical pathway |
title_short | Pancreatic cystic lesions: The value of contrast-enhanced endoscopic ultrasound to influence the clinical pathway |
title_sort | pancreatic cystic lesions: the value of contrast-enhanced endoscopic ultrasound to influence the clinical pathway |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4064160/ https://www.ncbi.nlm.nih.gov/pubmed/24955342 http://dx.doi.org/10.4103/2303-9027.131040 |
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