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Differentiation of pancreatic cysts with optical coherence tomography (OCT) imaging: an ex vivo pilot study

We demonstrate for the first time that optical coherence tomography (OCT) imaging can reliably distinguish between morphologic features of low risk pancreatic cysts (i.e., pseudocysts and serous cystadenomas) and high risk pancreatic cysts (i.e., mucinous cystic neoplasms and intraductal papillary m...

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Autores principales: Iftimia, Nicusor, Cizginer, Sevdenur, Deshpande, Vikram, Pitman, Martha, Tatli, Servet, Iftimia, Nicolae-Adrian, Hammer, Daniel X, Mujat, Mircea, Ustun, Teoman, Ferguson, R. Daniel, Brugge, William R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Optical Society of America 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3149535/
https://www.ncbi.nlm.nih.gov/pubmed/21833374
http://dx.doi.org/10.1364/BOE.2.002372
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author Iftimia, Nicusor
Cizginer, Sevdenur
Deshpande, Vikram
Pitman, Martha
Tatli, Servet
Iftimia, Nicolae-Adrian
Hammer, Daniel X
Mujat, Mircea
Ustun, Teoman
Ferguson, R. Daniel
Brugge, William R.
author_facet Iftimia, Nicusor
Cizginer, Sevdenur
Deshpande, Vikram
Pitman, Martha
Tatli, Servet
Iftimia, Nicolae-Adrian
Hammer, Daniel X
Mujat, Mircea
Ustun, Teoman
Ferguson, R. Daniel
Brugge, William R.
author_sort Iftimia, Nicusor
collection PubMed
description We demonstrate for the first time that optical coherence tomography (OCT) imaging can reliably distinguish between morphologic features of low risk pancreatic cysts (i.e., pseudocysts and serous cystadenomas) and high risk pancreatic cysts (i.e., mucinous cystic neoplasms and intraductal papillary mucinous neoplasms). In our study fresh pancreatectomy specimens (66) from patients with cystic lesions undergoing surgery were acquired and examined with OCT. A training set of 20 pathology-OCT correlated tissue specimens were used to develop criteria for differentiating between low and high risk cystic lesions. A separate (validation) set of 46 specimens were used to test the OCT criteria by three clinicians, blinded to histopathology findings. Histology was finally used as a ‘gold’ standard for testing OCT findings. OCT was able to reveal specific morphologic features of pancreatic cysts and thus to differentiate between low-risk and high-risk cysts with over 95% sensitivity and specificity. This pilot study suggests that OCT could be used by clinicians in the future to more reliably differentiate between benign and potentially malignant pancreatic cysts. However, in vivo use of OCT requires a probe that has to fit the bore of the pancreas biopsy needle. Therefore, we have developed such probes and planned to start an in vivo pilot study within the very near future.
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spelling pubmed-31495352011-08-10 Differentiation of pancreatic cysts with optical coherence tomography (OCT) imaging: an ex vivo pilot study Iftimia, Nicusor Cizginer, Sevdenur Deshpande, Vikram Pitman, Martha Tatli, Servet Iftimia, Nicolae-Adrian Hammer, Daniel X Mujat, Mircea Ustun, Teoman Ferguson, R. Daniel Brugge, William R. Biomed Opt Express Optics in Cancer Research We demonstrate for the first time that optical coherence tomography (OCT) imaging can reliably distinguish between morphologic features of low risk pancreatic cysts (i.e., pseudocysts and serous cystadenomas) and high risk pancreatic cysts (i.e., mucinous cystic neoplasms and intraductal papillary mucinous neoplasms). In our study fresh pancreatectomy specimens (66) from patients with cystic lesions undergoing surgery were acquired and examined with OCT. A training set of 20 pathology-OCT correlated tissue specimens were used to develop criteria for differentiating between low and high risk cystic lesions. A separate (validation) set of 46 specimens were used to test the OCT criteria by three clinicians, blinded to histopathology findings. Histology was finally used as a ‘gold’ standard for testing OCT findings. OCT was able to reveal specific morphologic features of pancreatic cysts and thus to differentiate between low-risk and high-risk cysts with over 95% sensitivity and specificity. This pilot study suggests that OCT could be used by clinicians in the future to more reliably differentiate between benign and potentially malignant pancreatic cysts. However, in vivo use of OCT requires a probe that has to fit the bore of the pancreas biopsy needle. Therefore, we have developed such probes and planned to start an in vivo pilot study within the very near future. Optical Society of America 2011-07-25 /pmc/articles/PMC3149535/ /pubmed/21833374 http://dx.doi.org/10.1364/BOE.2.002372 Text en ©2011 Optical Society of America http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 Unported License, which permits download and redistribution, provided that the original work is properly cited. This license restricts the article from being modified or used commercially.
spellingShingle Optics in Cancer Research
Iftimia, Nicusor
Cizginer, Sevdenur
Deshpande, Vikram
Pitman, Martha
Tatli, Servet
Iftimia, Nicolae-Adrian
Hammer, Daniel X
Mujat, Mircea
Ustun, Teoman
Ferguson, R. Daniel
Brugge, William R.
Differentiation of pancreatic cysts with optical coherence tomography (OCT) imaging: an ex vivo pilot study
title Differentiation of pancreatic cysts with optical coherence tomography (OCT) imaging: an ex vivo pilot study
title_full Differentiation of pancreatic cysts with optical coherence tomography (OCT) imaging: an ex vivo pilot study
title_fullStr Differentiation of pancreatic cysts with optical coherence tomography (OCT) imaging: an ex vivo pilot study
title_full_unstemmed Differentiation of pancreatic cysts with optical coherence tomography (OCT) imaging: an ex vivo pilot study
title_short Differentiation of pancreatic cysts with optical coherence tomography (OCT) imaging: an ex vivo pilot study
title_sort differentiation of pancreatic cysts with optical coherence tomography (oct) imaging: an ex vivo pilot study
topic Optics in Cancer Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3149535/
https://www.ncbi.nlm.nih.gov/pubmed/21833374
http://dx.doi.org/10.1364/BOE.2.002372
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