Review of the clinical, histological, and molecular aspects of pancreatic endocrine neoplasms

A. A. Gumbs, P. S. Moore, M. Falconi, C. Bassi, S. Beghelli, I. Modlin, A. Scarpa

Research output: Contribution to journalArticle

Abstract

Pancreatic endocrine neoplasms (PENs) are rare tumors, and little is known about their genetic and chromosomal alterations. Elucidation of the molecular events involved in PEN carcinogenesis has been hindered by the fact that PENs have been considered a single disease entity. The emergence of novel molecular characterization strategies has, however, made it apparent that these lesions exhibit diverse molecular fingerprints, which will facilitate the precise delineation of PEN prognosis, histopathology, and carcinogenesis.

Original languageEnglish
Pages (from-to)45-53
Number of pages9
JournalJournal of Surgical Oncology
Volume81
Issue number1
DOIs
Publication statusPublished - Sep 2002

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Keywords

  • Endocrine
  • Ki-67
  • MEN1
  • Pancreas
  • Tumors

ASJC Scopus subject areas

  • Surgery
  • Oncology

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