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“Invisible” pancreatic masses identified by EUS by the “ductal cutoff sign”
Making a tissue diagnosis of pancreatic adenocarcinoma is best accomplished by EUS and fine-needle aspiration (FNA) of the lesion. Typically, a dark, or “hypoechoic” mass will be seen, which presents an obvious target for FNA. For small lesions, computerized tomography (CT) may be negative, but the...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6482601/ https://www.ncbi.nlm.nih.gov/pubmed/30880727 http://dx.doi.org/10.4103/eus.eus_49_15 |
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author | Fairley, Kimberly J. Diehl, David L. Johal, Amitpal S. |
author_facet | Fairley, Kimberly J. Diehl, David L. Johal, Amitpal S. |
author_sort | Fairley, Kimberly J. |
collection | PubMed |
description | Making a tissue diagnosis of pancreatic adenocarcinoma is best accomplished by EUS and fine-needle aspiration (FNA) of the lesion. Typically, a dark, or “hypoechoic” mass will be seen, which presents an obvious target for FNA. For small lesions, computerized tomography (CT) may be negative, but the lesion is still almost always seen on EUS imaging. Rarely, a pancreatic mass will appear isoechoic on EUS imaging. We report three “invisible” pancreatic masses identified only by a cutoff in the pancreatic duct (PD) and/or common bile duct (CBD). No mass, isoechoic or otherwise, was seen. EUS-FNA was performed in the area of ductal narrowing, with a positive identification of adenocarcinoma in these cases. |
format | Online Article Text |
id | pubmed-6482601 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-64826012019-04-30 “Invisible” pancreatic masses identified by EUS by the “ductal cutoff sign” Fairley, Kimberly J. Diehl, David L. Johal, Amitpal S. Endosc Ultrasound Case Report Making a tissue diagnosis of pancreatic adenocarcinoma is best accomplished by EUS and fine-needle aspiration (FNA) of the lesion. Typically, a dark, or “hypoechoic” mass will be seen, which presents an obvious target for FNA. For small lesions, computerized tomography (CT) may be negative, but the lesion is still almost always seen on EUS imaging. Rarely, a pancreatic mass will appear isoechoic on EUS imaging. We report three “invisible” pancreatic masses identified only by a cutoff in the pancreatic duct (PD) and/or common bile duct (CBD). No mass, isoechoic or otherwise, was seen. EUS-FNA was performed in the area of ductal narrowing, with a positive identification of adenocarcinoma in these cases. Wolters Kluwer - Medknow 2019 2019-03-15 /pmc/articles/PMC6482601/ /pubmed/30880727 http://dx.doi.org/10.4103/eus.eus_49_15 Text en Copyright: © 2019 Spring Media Publishing Co. Ltd http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Case Report Fairley, Kimberly J. Diehl, David L. Johal, Amitpal S. “Invisible” pancreatic masses identified by EUS by the “ductal cutoff sign” |
title | “Invisible” pancreatic masses identified by EUS by the “ductal cutoff sign” |
title_full | “Invisible” pancreatic masses identified by EUS by the “ductal cutoff sign” |
title_fullStr | “Invisible” pancreatic masses identified by EUS by the “ductal cutoff sign” |
title_full_unstemmed | “Invisible” pancreatic masses identified by EUS by the “ductal cutoff sign” |
title_short | “Invisible” pancreatic masses identified by EUS by the “ductal cutoff sign” |
title_sort | “invisible” pancreatic masses identified by eus by the “ductal cutoff sign” |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6482601/ https://www.ncbi.nlm.nih.gov/pubmed/30880727 http://dx.doi.org/10.4103/eus.eus_49_15 |
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