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Molecular analysis with pancreaseq® in evaluation and management of pancreatic cysts: A cohort of 28 patients

OBJECTIVES: Herein, we present the PancreaSeq® results of 28 patients and emphasize the usefulness of molecular testing in evaluation of pancreatic cysts. MATERIAL AND METHODS: A total of 10 (35.7%) non-diagnostic, 6 (21.4%) negative, 5 (17.8%) atypical, and 7 (25%) were positive for mucinous cystic...

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Autores principales: Ardor, Gokce Deniz, Hanna, Helena, Ozalp, Bora, Nassar, Aziza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Scientific Scholar 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10481854/
https://www.ncbi.nlm.nih.gov/pubmed/37681071
http://dx.doi.org/10.25259/Cytojournal_28_2023
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author Ardor, Gokce Deniz
Hanna, Helena
Ozalp, Bora
Nassar, Aziza
author_facet Ardor, Gokce Deniz
Hanna, Helena
Ozalp, Bora
Nassar, Aziza
author_sort Ardor, Gokce Deniz
collection PubMed
description OBJECTIVES: Herein, we present the PancreaSeq® results of 28 patients and emphasize the usefulness of molecular testing in evaluation of pancreatic cysts. MATERIAL AND METHODS: A total of 10 (35.7%) non-diagnostic, 6 (21.4%) negative, 5 (17.8%) atypical, and 7 (25%) were positive for mucinous cystic neoplasm (MCN) pancreatic cyst aspirates were analyzed with PancreaSeq® at Mayo Clinic, Jacksonville between September 2021 and February 2023. RESULTS: Three non-diagnostic, two negative, three atypical, and two positive for MCN cysts were positive for KRAS and GNAS mutations. They were interpreted as intraductal papillary mucinous neoplasm (IPMN) with low risk for progression to high-grade dysplasia/adenocarcinoma. One negative case was positive for KRAS and GNAS mutation and RNF43 copy number alteration. It was interpreted as IPMN with a low risk of progression. Two non-diagnostic, one negative, and two positive for MCN cysts were positive for KRAS mutation. All were interpreted as IPMN/MCNs with low risk of progression. One positive for MCN case was positive for GNAS mutation and ALK fusion and one positive for MCN case was positive for GNAS mutation, ALK fusion, and RNF43 copy number alteration. Both were interpreted as IPMN and their risk of progression was interpreted as not well understood. One atypical case was positive for KRAS and TP53 mutation and was interpreted as IPMN/ MCNs with a high risk of progression. VHL mutation was present in one non-diagnostic case. It was interpreted as serous cystadenoma and the risk for progression was low. CONCLUSION: Molecular analysis of pancreatic cysts with PancreaSeq® is useful in accurate diagnosis, especially when cytologic material is non-diagnostic and helps improve patient management.
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spelling pubmed-104818542023-09-07 Molecular analysis with pancreaseq® in evaluation and management of pancreatic cysts: A cohort of 28 patients Ardor, Gokce Deniz Hanna, Helena Ozalp, Bora Nassar, Aziza Cytojournal Research Article OBJECTIVES: Herein, we present the PancreaSeq® results of 28 patients and emphasize the usefulness of molecular testing in evaluation of pancreatic cysts. MATERIAL AND METHODS: A total of 10 (35.7%) non-diagnostic, 6 (21.4%) negative, 5 (17.8%) atypical, and 7 (25%) were positive for mucinous cystic neoplasm (MCN) pancreatic cyst aspirates were analyzed with PancreaSeq® at Mayo Clinic, Jacksonville between September 2021 and February 2023. RESULTS: Three non-diagnostic, two negative, three atypical, and two positive for MCN cysts were positive for KRAS and GNAS mutations. They were interpreted as intraductal papillary mucinous neoplasm (IPMN) with low risk for progression to high-grade dysplasia/adenocarcinoma. One negative case was positive for KRAS and GNAS mutation and RNF43 copy number alteration. It was interpreted as IPMN with a low risk of progression. Two non-diagnostic, one negative, and two positive for MCN cysts were positive for KRAS mutation. All were interpreted as IPMN/MCNs with low risk of progression. One positive for MCN case was positive for GNAS mutation and ALK fusion and one positive for MCN case was positive for GNAS mutation, ALK fusion, and RNF43 copy number alteration. Both were interpreted as IPMN and their risk of progression was interpreted as not well understood. One atypical case was positive for KRAS and TP53 mutation and was interpreted as IPMN/ MCNs with a high risk of progression. VHL mutation was present in one non-diagnostic case. It was interpreted as serous cystadenoma and the risk for progression was low. CONCLUSION: Molecular analysis of pancreatic cysts with PancreaSeq® is useful in accurate diagnosis, especially when cytologic material is non-diagnostic and helps improve patient management. Scientific Scholar 2023-09-01 /pmc/articles/PMC10481854/ /pubmed/37681071 http://dx.doi.org/10.25259/Cytojournal_28_2023 Text en © 2023 Cytopathology Foundation Inc, Published by Scientific Scholar https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-Share Alike 4.0 License, which allows others to remix, transform, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Research Article
Ardor, Gokce Deniz
Hanna, Helena
Ozalp, Bora
Nassar, Aziza
Molecular analysis with pancreaseq® in evaluation and management of pancreatic cysts: A cohort of 28 patients
title Molecular analysis with pancreaseq® in evaluation and management of pancreatic cysts: A cohort of 28 patients
title_full Molecular analysis with pancreaseq® in evaluation and management of pancreatic cysts: A cohort of 28 patients
title_fullStr Molecular analysis with pancreaseq® in evaluation and management of pancreatic cysts: A cohort of 28 patients
title_full_unstemmed Molecular analysis with pancreaseq® in evaluation and management of pancreatic cysts: A cohort of 28 patients
title_short Molecular analysis with pancreaseq® in evaluation and management of pancreatic cysts: A cohort of 28 patients
title_sort molecular analysis with pancreaseq® in evaluation and management of pancreatic cysts: a cohort of 28 patients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10481854/
https://www.ncbi.nlm.nih.gov/pubmed/37681071
http://dx.doi.org/10.25259/Cytojournal_28_2023
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