Metabolomic and Lipidomic Profiling of Plasma and Cyst Fluid Allows the Detection and Characterization of Pancreatic Intraductal Papillary Mucinous Neoplasms

2018 ◽  
Author(s):  
Rogier Gaiser ◽  
Alberto Pessia ◽  
Zeeshan Ateeb ◽  
Haleh Davanian ◽  
Carlos Fernández Moro ◽  
...  
Pancreatology ◽  
2008 ◽  
Vol 8 (3) ◽  
pp. 277-284 ◽  
Author(s):  
Martha Bishop Pitman ◽  
Paul J. Michaels ◽  
Vikram Deshpande ◽  
William R. Brugge ◽  
Brenna C. Bounds

2019 ◽  
Vol 228 (5) ◽  
pp. 721-729 ◽  
Author(s):  
Ajay V. Maker ◽  
Vincent Hu ◽  
Shrihari S. Kadkol ◽  
Lenny Hong ◽  
William Brugge ◽  
...  

2008 ◽  
Vol 15 (2) ◽  
pp. 169-177 ◽  
Author(s):  
Noritoshi Kobayashi ◽  
Masahiko Inamori ◽  
Koji Fujita ◽  
Toshio Fujisawa ◽  
Nobutaka Fujisawa ◽  
...  

2010 ◽  
Vol 18 (1) ◽  
pp. 199-206 ◽  
Author(s):  
Ajay V. Maker ◽  
Nora Katabi ◽  
Mithat Gonen ◽  
Ronald P. DeMatteo ◽  
Michael I. D’Angelica ◽  
...  

2020 ◽  
Vol 21 (3) ◽  
pp. 1147
Author(s):  
Scarlett Hao ◽  
Caitlin Takahashi ◽  
Rebecca A. Snyder ◽  
Alexander A. Parikh

A significant proportion of patients with intraductal papillary mucinous neoplasms (IPMNs) undergo surgical resection in order to prevent or treat pancreatic cancer at the risk of significant perioperative morbidity. Efforts have been made to stratify the potential risk of malignancy based on the clinical and radiographic features of IPMN to delineate which cysts warrant resection versus observation. An analysis of the cyst fluid obtained by preoperative endoscopic examination appears to be correlative of cyst type and risk, whereas serum markers and radiographic findings have not yet reached a level of sensitivity or specificity that proves they are clinically meaningful. In this review, we investigate the current cyst fluid analysis studies and present those that have shown promise in effectively stratifying high-risk versus low-risk lesions. While new cyst fluid markers continue to be identified, additional efforts in testing panels and marker composites in conjunction with clinical algorithms have also shown promise in distinguishing dysplasia and the risk of malignancy. These should be tested prospectively in order to determine their role in guiding the surveillance of low-risk lesions and to evaluate the new markers detected by proteomics and genetic sequencing.


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