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Original Articles| Volume 54, ISSUE 5, P595-599, November 2001

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Pancreatic intraductal sampling during ERCP in patients with chronic pancreatitis and pancreatic cancer: cytologic studies and k-ras-2 codon 12 molecular analysis in 47 cases

  • Vittorio Pugliese
    Affiliations
    Center for Gastrointestinal Endoscopy, the Department of Oncology, Biology, and Genetics, University of Genoa, and from the Services of Digestive Endoscopy and Gastroenterology, of Pathology, and of Immunogenetics, National Cancer Institute, Genova, Italy
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  • Natalia Pujic
    Affiliations
    Center for Gastrointestinal Endoscopy, the Department of Oncology, Biology, and Genetics, University of Genoa, and from the Services of Digestive Endoscopy and Gastroenterology, of Pathology, and of Immunogenetics, National Cancer Institute, Genova, Italy
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  • Sebastiano Saccomanno
    Affiliations
    Center for Gastrointestinal Endoscopy, the Department of Oncology, Biology, and Genetics, University of Genoa, and from the Services of Digestive Endoscopy and Gastroenterology, of Pathology, and of Immunogenetics, National Cancer Institute, Genova, Italy
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  • Beatrice Gatteschi
    Affiliations
    Center for Gastrointestinal Endoscopy, the Department of Oncology, Biology, and Genetics, University of Genoa, and from the Services of Digestive Endoscopy and Gastroenterology, of Pathology, and of Immunogenetics, National Cancer Institute, Genova, Italy
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  • Cinzia Pera
    Affiliations
    Center for Gastrointestinal Endoscopy, the Department of Oncology, Biology, and Genetics, University of Genoa, and from the Services of Digestive Endoscopy and Gastroenterology, of Pathology, and of Immunogenetics, National Cancer Institute, Genova, Italy
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  • Hugo Aste
    Affiliations
    Center for Gastrointestinal Endoscopy, the Department of Oncology, Biology, and Genetics, University of Genoa, and from the Services of Digestive Endoscopy and Gastroenterology, of Pathology, and of Immunogenetics, National Cancer Institute, Genova, Italy
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  • Giovanni Battist Ferrara
    Affiliations
    Center for Gastrointestinal Endoscopy, the Department of Oncology, Biology, and Genetics, University of Genoa, and from the Services of Digestive Endoscopy and Gastroenterology, of Pathology, and of Immunogenetics, National Cancer Institute, Genova, Italy
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  • Guido Nicolò
    Affiliations
    Center for Gastrointestinal Endoscopy, the Department of Oncology, Biology, and Genetics, University of Genoa, and from the Services of Digestive Endoscopy and Gastroenterology, of Pathology, and of Immunogenetics, National Cancer Institute, Genova, Italy
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      Abstract

      Background: A preoperative tissue diagnosis of pancreatic cancer is desirable but difficult to obtain. Methods: Pancreatic brush cytology, salvage cytology, and collection of pancreatic juice were attempted prospectively during ERCP in 34 patients with pancreatic cancer and 11 with chronic pancreatitis. K-ras-2 codon 12 was analyzed for presence and type of point mutations. Results: Brush cytology coupled with salvage cytology had a sensitivity of 74%. The addition of cytologic analysis of pancreatic juice did not substantially improve sensitivity (76%). K-ras-2 was mutated in both cancer (87%) and pancreatitis (40%). The specificity for cytology was 100% and for K-ras-2 mutations 60%. Combining cytology with mutation analysis increased sensitivity to 93% but reduced the positive predictive value. The negative predictive value never exceeded 75%. None of the patients with chronic pancreatitis had cancer develop (median follow-up 60 months). Conclusions: Pancreatic ductal brushing with salvage cytology is useful in the diagnosis of cancer, whereas cytologic analysis of pancreatic juice can be abandoned. At present, K-ras-2 mutation is not useful for differentiating pancreatic cancer from chronic pancreatitis or the identification of patients with chronic pancreatitis at risk for malignant transformation. (Gastrointest Endosc 2001;54:595-9.)
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