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

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...

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Veröffentlicht in:Journal of surgical oncology 2002-09, Vol.81 (1), p.45-53
Hauptverfasser: Gumbs, A.A., Moore, P.S., Falconi, M., Bassi, C., Beghelli, S., Modlin, I., Scarpa, A.
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Sprache:eng
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Zusammenfassung: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. J. Surg. Oncol. 2002;81:45–53. © 2002 Wiley‐Liss, Inc.
ISSN:0022-4790
1096-9098
DOI:10.1002/jso.10142