Pancreatic neuroendocrine tumors: Clinical features, diagnosis and medical treatment: Advances

Tetsuhide Ito, Hisato Igarashi, Robert T. Jensen

研究成果: Contribution to journalReview article査読

103 被引用数 (Scopus)

抄録

Pancreatic neuroendocrine tumors (pNETs) comprise with gastrointestinal carcinoids, the main groups of gastrointestinal neuroendocrine tumors (GI-NETs). Although these two groups of GI-NETs share many features including histological aspects; over-/ectopic expression of somatostatin receptors; the ability to ectopically secrete hormones/peptides/amines which can result in distinct functional syndromes; similar approaches used for tumor localization and some aspects of treatment, it is now generally agreed they should be considered separate. They differ in their pathogenesis, hormonal syndromes produced, many aspects of biological behaviour and most important, in their response to certain anti-tumour treatment (chemotherapy, molecular targeted therapies). In this chapter the clinical features of the different types of pNETs will be considered as well as aspects of their diagnosis and medical treatment of the hormone-excess state. Emphasis will be on controversial areas or recent advances. The other aspects of the management of these tumors (surgery, treatment of advanced disease, tumor localization) are not dealt with here, because they are covered in other chapters in this volume.

本文言語英語
ページ(範囲)737-753
ページ数17
ジャーナルBest Practice and Research: Clinical Gastroenterology
26
6
DOI
出版ステータス出版済み - 12 2012

All Science Journal Classification (ASJC) codes

  • Gastroenterology

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