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      A REVISED CLASSIFICATION SYSTEM AND RECOMMENDATIONS FROM THE BALTIMORE CONSENSUS MEETING FOR NEOPLASTIC PRECURSOR LESIONS IN THE PANCREAS

      research-article
      , MD 1 , , MD, PhD 2 , , MD, PhD 3 , , MD 4 , , MD 5 , , MD 6 , , MD, PhD 7 , , MD 8 , , MD 3 , , MD 3 , , MD 9 , , MD 1 , , MD 10 , , MD 4 , , MD 11 , , MD 12 , , MD, PhD 7 , , MD 13 , , MD, PhD 14 , , MD 15 , , MD, PhD 16 , , MD 17 , , MD, PhD 18
      The American journal of surgical pathology
      Pancreatic intraepithelial neoplasia (PanIN), intraductal papillary mucinous neoplasm (IPMN), mucinous cystic neoplasm (MCN), precursor, adenocarcinoma, atypical flat lesions (AFL)

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          Abstract

          International experts met to discuss recent advances and to revise the 2004 recommendations for assessing and reporting precursor lesions to invasive carcinomas of the pancreas, including pancreatic intraepithelial neoplasia (PanIN), intraductal papillary mucinous neoplasm (IPMN), mucinous cystic neoplasm, and other lesions. Consensus recommendations include the following: 1) To improve concordance and to align with practical consequences, a two-tiered system (low vs. high-grade) is proposed for all precursor lesions, with the provision that the current PanIN-2 and neoplasms with intermediate-grade dysplasia now be categorized as low-grade. Thus, “high-grade dysplasia” is to be reserved for only the uppermost end of the spectrum (“carcinoma in situ” type lesions). 2) Current data indicate that PanIN of any grade at a margin of a resected pancreas with invasive carcinoma does not have prognostic implications; the clinical significance of dysplasia at a margin in a resected pancreas with IPMN lacking invasive carcinoma remains to be determined. 3) Intraductal lesions 0.5–1 cm can be either large PanINs or small IPMNs. The term “incipient IPMN” should be reserved for lesions in this size with intestinal- or oncocytic-papillae or GNAS mutations. 4) Measurement of the distance between an IPMN and invasive carcinoma and sampling of intervening tissue are recommended to assess concomitant versus associated status. Conceptually, concomitant invasive carcinoma (in contrast with the “associated” group) ought to be genetically distinct from an IPMN elsewhere in the gland. 5) “Intraductal spread of invasive carcinoma” (aka, “colonization”) is recommended to describe lesions of invasive carcinoma invading back into and extending along the duct system, which may morphologically mimic high-grade PanIN or even IPMN. 6) “ Simple mucinous cyst” is recommended to describe cysts > 1 cm having gastric-type flat mucinous lining at most minimal atypia without ovarian-type stroma to distinguish them from IPMN. 7) Human lesions resembling the acinar-to-ductal metaplasia and atypical flat lesions of genetically engineered mouse models exist and may reflect an alternate pathway of carcinogenesis; however, their biological significance requires further study. These revised recommendations are expected to improve our management and understanding of precursor lesions in the pancreas.

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          Author and article information

          Journal
          7707904
          470
          Am J Surg Pathol
          Am. J. Surg. Pathol.
          The American journal of surgical pathology
          0147-5185
          1532-0979
          1 August 2015
          December 2015
          01 December 2016
          : 39
          : 12
          : 1730-1741
          Affiliations
          [1 ]Memorial Sloan Kettering Cancer Center, NY
          [2 ]Asan Medical Center, University of Ulsan College of Medicine, Korea
          [3 ]The Sol Goldman Pancreatic Cancer Research Center, Department of Pathology, Johns Hopkins University School of Medicine, MD
          [4 ]Emory University Hospital, GA
          [5 ]Medica Sur Clinic and Foundation, Mexico
          [6 ]University of Glasgow, UK
          [7 ]University Medical Center Utrecht, The Netherlands
          [8 ]Jichi Medical University, Japan
          [9 ]Cancer Institute, Japanese Foundation for Cancer Research, Japan
          [10 ]Technical University Munich, Germany
          [11 ]Dartmouth-Hitchcock Medical Center, NH
          [12 ]University of Bonn, Germany
          [13 ]Hakujikai Memorial Hospital, Japan
          [14 ]Kyoto University, Japan
          [15 ]Hôpital Cochin, France
          [16 ]National Cancer Center Research Institute, Japan
          [17 ]Heinrich-Heine University and University Hospital of Düsseldorf, Germany
          [18 ]Tokyo Women’s Medical University, Japan
          Author notes
          Corresponding Authors: Toru Furukawa, MD, PhD, Institute for Integrated Medical Sciences, Tokyo Women’s Medical University, 8-1 Kawada-cho, Shinjuku-ku, Tokyo 162-8666, Japan, Phone: +81-3-3353-8111, Fax: +81-3-5269-7667, furukawa.toru@ 123456twmu.ac.jp . Irene Esposito, MD, Institute of Pathology, Heinrich-Heine University and University Hospital of Düsseldorf, Moorenstr. 5, 40225 Düsseldorf Germany, Phone: +49-211-811-8339, Fax: +49-211-811-8353, irene_esposito@ 123456gmx.de
          [*]

          Co-contributing first authors

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          Co-contributing corresponding authors

          Article
          PMC4646710 PMC4646710 4646710 nihpa709550
          10.1097/PAS.0000000000000533
          4646710
          26559377
          1684ce23-26d8-4cfd-8983-5dd9e0886346
          History
          Categories
          Article

          atypical flat lesions (AFL),Pancreatic intraepithelial neoplasia (PanIN),intraductal papillary mucinous neoplasm (IPMN),mucinous cystic neoplasm (MCN),precursor,adenocarcinoma

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