Surgical treatment of endocrine pancreatic tumours.

Abstract:

:Endocrine pancreatic tumours (EPTs) are uncommon, with a major challenge to alert physicians to their recognition and requirements of treatment. Functioning EPTs cause well-known clinical syndromes of hormone excess. Insulinomas, gastrinomas and glucagonomas are most common; vipomas and somatostatinomas are rare. EPTs also occur as non-functioning lesions without symptoms of hormone excess occasionally with ectopic hormone, such as ACTH and Cushing syndrome as a late complication. The majority of EPTs are sporadic, but they may also be part of a multiple endocrine neoplasia type 1 syndrome or rarely the von Hippel-Lindau syndrome. EPTs have been of great interest to endocrine surgeons and we have, during recent years, witnessed continuing advances in diagnosis, imaging and treatment of the different tumour entities. It has become obvious that surgical treatment of these tumours is of increased concern and can have a marked impact on symptoms and survival.

journal_name

Neuroendocrinology

journal_title

Neuroendocrinology

authors

Akerström G,Hellman P,Hessman O,Osmak L

doi

10.1159/000080744

subject

Has Abstract

pub_date

2004-01-01 00:00:00

pages

62-6

eissn

0028-3835

issn

1423-0194

pii

80744

journal_volume

80 Suppl 1

pub_type

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