2015
DOI: 10.1016/j.gie.2014.08.023
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Differentiation of pancreatic ductal adenocarcinoma from other neoplastic solid pancreatic lesions: a tertiary oncology center experience

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Cited by 17 publications
(9 citation statements)
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“…Of the 34 false negative tests 38% had a final diagnosis of benign lesions and 62% had a diagnosis of another malignancy at the time of surgical resection. Additionally, when the presence of atypical cells were considered a negative test, specificity was includingcomparable to the literature (90%), but the sensitivity of diagnosing PDAC when utilizing EUS-FNA was significantly lower (68.2%) compared to commonly reported sensitivities of 80-85% [4][5][16][17][18] . Another study reported very low incidence of false positive diagnosis (0-5%) when using EUS-FNA as a diagnostic tool for PDAC [12] .…”
Section: Discussionmentioning
confidence: 66%
See 1 more Smart Citation
“…Of the 34 false negative tests 38% had a final diagnosis of benign lesions and 62% had a diagnosis of another malignancy at the time of surgical resection. Additionally, when the presence of atypical cells were considered a negative test, specificity was includingcomparable to the literature (90%), but the sensitivity of diagnosing PDAC when utilizing EUS-FNA was significantly lower (68.2%) compared to commonly reported sensitivities of 80-85% [4][5][16][17][18] . Another study reported very low incidence of false positive diagnosis (0-5%) when using EUS-FNA as a diagnostic tool for PDAC [12] .…”
Section: Discussionmentioning
confidence: 66%
“…Previous studies have only separately evaluated the efficiency of EUS-FNA for diagnosing neuroendocrine tumors [9][10][11] , cystic neoplasms, such as intraductal papillary mucinous neoplasms (IPMN) [12][13][14][15] , or PDAC [16][17][18] .…”
Section: Introductionmentioning
confidence: 99%
“…Further observation of 3 separate periods of 100 pancreatic EUS-FNA following basic skills acquisition demonstrated further improvement in terms of a decreasing number of diagnostic needle passes 7 and decreasing adverse events in period 3 compared to periods 1 and 2 [144]. A 7-year experience in pancreatic EUS-FNA showed a significant correlation between years of operator experience and the mean of annual EUS examinations in the preceding 3 years with fewer needle passes [146,147]. A similar effect of cumulative EUS-FNA experience over a 13-year period on the diagnostic accuracy of pancreatic EUS-FNA was also reported, representing a joint learning curve of both endosonographers and cytopathologists [148].…”
Section: Learning Curve and Minimum Number Of Supervised Proceduresmentioning
confidence: 89%
“…In specialized tertiary referral centers for EUS-FNA, 13 % [148] to 21 % [194] of focal pancreatic lesions referred for cytopathological diagnosis turn out to be benign, often focal chronic and autoimmune pancreatitis. In the case of solid pancreatic neoplasms, 12 % to 25 % turn out to be non-PDAC (e. g. neuroendocrine tumors, pancreatic metastases, mesenchymal tumors, lymphoma, solid pseudopapillary neoplasia) [146,148,194,596]. The ratio of non-PDAC to PDAC is inversely related to the diameter of the tumor.…”
Section: Solid Pancreatic Lesionsmentioning
confidence: 99%
“…Pancreatic ductal adenocarcinoma accounts for nearly 90% of solid pancreatic masses. The remaining 10–15% is comprised of PanNET and metastases to the pancreas from other sites . EUS‐guided FNA has become routine in the work up of newly identified pancreatic masses (solid or cystic).…”
Section: Discussionmentioning
confidence: 99%