Frequency and Significance of Abnormal Pancreatic Imaging in Patients with BRCA1 and BRCA2 Genetic Mutations

Objective. Pancreatic adenocarcinoma is typically diagnosed in advanced stages resulting in a significant reduction in the number of patients who are candidates for surgical resection. Although the majority of cases are believed to occur sporadically, about 10% show familial clustering and studies h...

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Main Authors: Elie Chahla, Antonio Cheesman, Suzanne M. Mahon, Robert W. Garrett, Ben P. Bradenham, Theresa L. Schwartz, Louay Omran, Jason R. Taylor, Samer Alkaade
Format: Article
Language:English
Published: Wiley 2016-01-01
Series:Scientifica
Online Access:http://dx.doi.org/10.1155/2016/5619358
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author Elie Chahla
Antonio Cheesman
Suzanne M. Mahon
Robert W. Garrett
Ben P. Bradenham
Theresa L. Schwartz
Louay Omran
Jason R. Taylor
Samer Alkaade
author_facet Elie Chahla
Antonio Cheesman
Suzanne M. Mahon
Robert W. Garrett
Ben P. Bradenham
Theresa L. Schwartz
Louay Omran
Jason R. Taylor
Samer Alkaade
author_sort Elie Chahla
collection DOAJ
description Objective. Pancreatic adenocarcinoma is typically diagnosed in advanced stages resulting in a significant reduction in the number of patients who are candidates for surgical resection. Although the majority of cases are believed to occur sporadically, about 10% show familial clustering and studies have identified an increased frequency of BRCA germline mutations. The role of screening for pancreatic adenocarcinoma in these populations is unclear. Our study aims to identify the abnormal pancreatic imaging findings in BRCA1 and BRCA2 mutation carriers. Methods. A retrospective review of patient medical records with known BRCA1 and BRCA2 mutations was conducted. Data was collected and all available abdominal imaging studies were reviewed. Results. A total of 66 patients were identified, 36 with BRCA1 and 30 with BRCA2 mutations. Only 20/66 (30%) had abdominal imaging (14 BRCA1 and 6 BRCA2 patients). Of those patients with abdominal imaging, abnormal pancreatic imaging findings were detected in 7/20 (35%) cases. Conclusion. Our study shows a high incidence of abnormal pancreatic imaging findings in patients with BRCA genetic mutations (35%). Larger studies are needed to further define the role of pancreatic cancer screening and the significance of abnormal imaging findings in BRCA1 and BRCA2 mutation carriers.
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spelling doaj-art-517c7394e8bb453cb38b912cbbe483a32025-02-03T01:31:09ZengWileyScientifica2090-908X2016-01-01201610.1155/2016/56193585619358Frequency and Significance of Abnormal Pancreatic Imaging in Patients with BRCA1 and BRCA2 Genetic MutationsElie Chahla0Antonio Cheesman1Suzanne M. Mahon2Robert W. Garrett3Ben P. Bradenham4Theresa L. Schwartz5Louay Omran6Jason R. Taylor7Samer Alkaade8Division of Gastroenterology and Hepatology, Saint Louis University School of Medicine, St. Louis, MO 63110, USADepartment of Internal Medicine, Saint Louis University School of Medicine, St. Louis, MO 63110, USADivision of Hematology and Oncology, Saint Louis University School of Medicine, St. Louis, MO 63110, USADepartment of Radiology, Saint Louis University School of Medicine, St. Louis, MO 63110, USADivision of Gastroenterology and Hepatology, Saint Louis University School of Medicine, St. Louis, MO 63110, USADepartment of General Surgery, Saint Louis University School of Medicine, St. Louis, MO 63110, USADivision of Gastroenterology and Hepatology, Saint Louis University School of Medicine, St. Louis, MO 63110, USADivision of Gastroenterology and Hepatology, Saint Louis University School of Medicine, St. Louis, MO 63110, USADivision of Gastroenterology and Hepatology, Saint Louis University School of Medicine, St. Louis, MO 63110, USAObjective. Pancreatic adenocarcinoma is typically diagnosed in advanced stages resulting in a significant reduction in the number of patients who are candidates for surgical resection. Although the majority of cases are believed to occur sporadically, about 10% show familial clustering and studies have identified an increased frequency of BRCA germline mutations. The role of screening for pancreatic adenocarcinoma in these populations is unclear. Our study aims to identify the abnormal pancreatic imaging findings in BRCA1 and BRCA2 mutation carriers. Methods. A retrospective review of patient medical records with known BRCA1 and BRCA2 mutations was conducted. Data was collected and all available abdominal imaging studies were reviewed. Results. A total of 66 patients were identified, 36 with BRCA1 and 30 with BRCA2 mutations. Only 20/66 (30%) had abdominal imaging (14 BRCA1 and 6 BRCA2 patients). Of those patients with abdominal imaging, abnormal pancreatic imaging findings were detected in 7/20 (35%) cases. Conclusion. Our study shows a high incidence of abnormal pancreatic imaging findings in patients with BRCA genetic mutations (35%). Larger studies are needed to further define the role of pancreatic cancer screening and the significance of abnormal imaging findings in BRCA1 and BRCA2 mutation carriers.http://dx.doi.org/10.1155/2016/5619358
spellingShingle Elie Chahla
Antonio Cheesman
Suzanne M. Mahon
Robert W. Garrett
Ben P. Bradenham
Theresa L. Schwartz
Louay Omran
Jason R. Taylor
Samer Alkaade
Frequency and Significance of Abnormal Pancreatic Imaging in Patients with BRCA1 and BRCA2 Genetic Mutations
Scientifica
title Frequency and Significance of Abnormal Pancreatic Imaging in Patients with BRCA1 and BRCA2 Genetic Mutations
title_full Frequency and Significance of Abnormal Pancreatic Imaging in Patients with BRCA1 and BRCA2 Genetic Mutations
title_fullStr Frequency and Significance of Abnormal Pancreatic Imaging in Patients with BRCA1 and BRCA2 Genetic Mutations
title_full_unstemmed Frequency and Significance of Abnormal Pancreatic Imaging in Patients with BRCA1 and BRCA2 Genetic Mutations
title_short Frequency and Significance of Abnormal Pancreatic Imaging in Patients with BRCA1 and BRCA2 Genetic Mutations
title_sort frequency and significance of abnormal pancreatic imaging in patients with brca1 and brca2 genetic mutations
url http://dx.doi.org/10.1155/2016/5619358
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