Our system is currently under heavy load due to increased usage. We're actively working on upgrades to improve performance. Thank you for your patience.
2004
DOI: 10.1016/j.jss.2003.12.007
|View full text |Cite
|
Sign up to set email alerts
|

Pancreatic endocrine tumors

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1

Citation Types

1
96
1

Year Published

2005
2005
2016
2016

Publication Types

Select...
8
1

Relationship

0
9

Authors

Journals

citations
Cited by 137 publications
(98 citation statements)
references
References 180 publications
(214 reference statements)
1
96
1
Order By: Relevance
“…The diagnosis is confirmed by the demonstration of inappropriately elevated insulin and proinsulin levels associated with serum glucose values of less than 50 mg/dL during 48 hour fast period. 3,4 Insulinoma may be associated with a hereditary syndrome in nearly 10% of patients, the most common being multiple endocrine neoplasia type 1 (MEN1) 5 . Insulinomas are evenly distributed throughout the pancreas and are usually less than 2 cm in size in approximately 90% of cases 1 .…”
Section: Introductionmentioning
confidence: 99%
“…The diagnosis is confirmed by the demonstration of inappropriately elevated insulin and proinsulin levels associated with serum glucose values of less than 50 mg/dL during 48 hour fast period. 3,4 Insulinoma may be associated with a hereditary syndrome in nearly 10% of patients, the most common being multiple endocrine neoplasia type 1 (MEN1) 5 . Insulinomas are evenly distributed throughout the pancreas and are usually less than 2 cm in size in approximately 90% of cases 1 .…”
Section: Introductionmentioning
confidence: 99%
“…The overall prognosis and long-term survival for PNET patients are far better than for patients with exocrine pancreatic cancer [13,14]. The overall 5-year survival rate is in the range of 30% in NF-PNETs to 97% in insulinoma, one category of F-PNET [15].…”
Section: Introductionmentioning
confidence: 99%
“…PETs occur in adults of all age groups, with no sex differences (prevalence of w1 in 100 000 individuals) and are extremely rare in children. PETs may be isolated or occur in association with other endocrine tumours in the multiple endocrine neoplasia type 1 (MEN-1) syndrome or, more rarely, in the von Hippel-Lindau syndrome (Mansour & Chen 2004, Oberg & Eriksson 2005. PETs, like all NETs, are categorized on the basis of their clinical manifestations into functioning and non-functioning tumours.…”
Section: Introductionmentioning
confidence: 99%