Literature DB >> 11420467

The immunohistochemical mucin expression pattern distinguishes different types of intraductal papillary mucinous neoplasms of the pancreas and determines their relationship to mucinous noncystic carcinoma and ductal adenocarcinoma.

J Lüttges1, G Zamboni, D Longnecker, G Klöppel.   

Abstract

Intraductal papillary-mucinous neoplasms of the pancreas seem to comprise various types, whose relationship to ductal adenocarcinoma and mucinous noncystic carcinoma is unclear. We analyzed the mucin immunophenotype and the DPC4/SMAD4 expression in intraductal papillary-mucinous neoplasms, ductal carcinomas, and mucinous noncystic carcinomas to define features that may help to distinguish between different types of intraductal papillary-mucinous neoplasms and to establish their relationship to other neoplasms of the exocrine pancreas. A series of 51 intraductal papillary-mucinous neoplasms, three mucinous noncystic carcinomas (two with an intraductal component), and 35 ductal adenocarcinomas were screened immunohistochemically for their expression of MUC1, MUC2, MUC5, and DPC4/SMAD4. All intraductal papillary-mucinous neoplasms and mucinous noncystic carcinomas were positive for MUC5. Thirty-two intraductal papillary-mucinous neoplasms and three mucinous noncystic carcinomas abundantly expressed MUC2 but no (or only little) MUC1. The remaining intraductal papillary-mucinous neoplasms showed either mainly MUC1 expression or focal MUC1 and MUC2 expression. All ductal carcinomas but one were MUC2 negative and MUC1 and MUC5 positive. DPC4 was not expressed in two intraductal papillary-mucinous neoplasms that showed a tubular invasion pattern. Twelve of 23 ductal adenocarcinomas were DPC4 positive. Intraductal papillary-mucinous neoplasms can be divided into at least three different mucin immunophenotypes. The first and largest group of intraductal papillary-mucinous neoplasms and mucinous noncystic carcinomas is MUC1 negative and MUC2 positive and probably forms one tumor entity. The second group seems to be related to ductal carcinoma because of its MUC1 positivity in the absence or very weak MUC2 staining. The third group shows focal MUC1/MUC2 expression and is characterized by oncocytic histology.

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Year:  2001        PMID: 11420467     DOI: 10.1097/00000478-200107000-00014

Source DB:  PubMed          Journal:  Am J Surg Pathol        ISSN: 0147-5185            Impact factor:   6.394


  65 in total

1.  Pancreatic intraductal tubulopapillary neoplasm is genetically distinct from intraductal papillary mucinous neoplasm and ductal adenocarcinoma.

Authors:  Olca Basturk; Michael F Berger; Hiroshi Yamaguchi; Volkan Adsay; Gokce Askan; Umesh K Bhanot; Ahmet Zehir; Fatima Carneiro; Seung-Mo Hong; Giuseppe Zamboni; Esra Dikoglu; Vaidehi Jobanputra; Kazimierz O Wrzeszczynski; Serdar Balci; Peter Allen; Naoki Ikari; Shoko Takeuchi; Hiroyuki Akagawa; Atsushi Kanno; Tooru Shimosegawa; Takanori Morikawa; Fuyuhiko Motoi; Michiaki Unno; Ryota Higuchi; Masakazu Yamamoto; Kyoko Shimizu; Toru Furukawa; David S Klimstra
Journal:  Mod Pathol       Date:  2017-08-04       Impact factor: 7.842

2.  Intraductal papillary mucinous neoplasm (IPMN) of the gastric-type with focal nodular growth of the arborizing papillae: a case of high-grade transformation of the gastric-type IPMN.

Authors:  Shinichi Ban; Yoshihisa Naitoh; Fumihiro Ogawa; Yoshihiko Shimizu; Michio Shimizu; Akihiro Yasumoto; Isamu Koyama
Journal:  Virchows Arch       Date:  2006-04-26       Impact factor: 4.064

3.  Intraductal papillary mucinous neoplasms of the pancreas: pathology and molecular genetics.

Authors:  N Volkan Adsay
Journal:  J Gastrointest Surg       Date:  2002 Sep-Oct       Impact factor: 3.452

4.  aRNA-longSAGE: a new approach to generate SAGE libraries from microdissected cells.

Authors:  Anna M Heidenblut; Jutta Lüttges; Malte Buchholz; Christian Heinitz; Jeppe Emmersen; Kåre Lehmann Nielsen; Pat Schreiter; Manfred Souquet; Sandra Nowacki; Ulrike Herbrand; Günter Klöppel; Wolff Schmiegel; Thomas Gress; Stephan A Hahn
Journal:  Nucleic Acids Res       Date:  2004-09-15       Impact factor: 16.971

Review 5.  [Pathology and classification of intraductal papillary mucinous neoplasms of the pancreas].

Authors:  A M Schlitter; I Esposito
Journal:  Chirurg       Date:  2012-02       Impact factor: 0.955

6.  Multicentric invasive carcinomas derived from intraductal papillary mucinous neoplasm (IPMN) of the pancreas: report of a case.

Authors:  Yoshihisa Naitoh; Shinichi Ban; Chouji Tsuchiya; Yoshiaki Sugiura; Michio Shimizu
Journal:  Virchows Arch       Date:  2007-02-28       Impact factor: 4.064

7.  Gene expression profiles of microdissected pancreatic ductal adenocarcinoma.

Authors:  Robert Grützmann; Melanie Foerder; Ingo Alldinger; Eike Staub; Thomas Brümmendorf; Stefan Röpcke; Xinzhong Li; Glen Kristiansen; Ralf Jesenofsky; Ralf Jesnowski; Bence Sipos; Matthias Löhr; Jutta Lüttges; Detlef Ockert; Günter Klöppel; Hans Detlev Saeger; Christian Pilarsky
Journal:  Virchows Arch       Date:  2003-08-27       Impact factor: 4.064

8.  Quantitative assessment of the diagnostic role of MUC1 in pancreatic ductal adenocarcinoma.

Authors:  Siliang Wang; Xiaodong Chen; Meiyue Tang
Journal:  Tumour Biol       Date:  2014-06-11

9.  Intraductal papillary mucinous neoplasm of the pancreas with loss of mismatch repair in a patient with Lynch syndrome.

Authors:  Jennifer A Sparr; Prathap Bandipalliam; Mark S Redston; Sapna Syngal
Journal:  Am J Surg Pathol       Date:  2009-02       Impact factor: 6.394

Review 10.  Morphogenesis of pancreatic cancer: role of pancreatic intraepithelial neoplasia (PanINs).

Authors:  Jan-Bart M Koorstra; Georg Feldmann; Nils Habbe; Anirban Maitra
Journal:  Langenbecks Arch Surg       Date:  2008-02-19       Impact factor: 3.445

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