ISLET-CELL CARCINOMA OF THE PANCREAS

Citation
Cy. Lo et al., ISLET-CELL CARCINOMA OF THE PANCREAS, World journal of surgery, 20(7), 1996, pp. 878-884
Citations number
27
Categorie Soggetti
Surgery
Journal title
ISSN journal
03642313
Volume
20
Issue
7
Year of publication
1996
Pages
878 - 884
Database
ISI
SICI code
0364-2313(1996)20:7<878:ICOTP>2.0.ZU;2-K
Abstract
Islet cell carcinoma (ICC) of the pancreas is a rare, indolent maligna ncy associated with higher resectability rate and better survival than ductal carcinoma. This retrospective study presents results of surgic al treatment from a single institution. From 1985 through 1993 a total of 64 patients (36 men, 28 women) were surgically treated for ICC. Ag es ranged from 22 to 80 years (median 55 years) with a median postoper ative follow-up of 39 months (range 10-97 months). Of the 64 patients, 30 (47%) had functioning and 33 (53%) nonfunctioning tumors. Gastrino ma (n = 11) followed by glucagonoma (n = 6) and insulinoma (n = 4) wer e the most common functioning tumors. In the patients undergoing a lab oratory study, 67% of the nonfunctioning tumors had elevated peptide h ormone levels. Potentially curative resections were performed in 17 pa tients (26%), palliative procedures in 35 (55%), and exploratory lapar otomy alone in 12 (19%). One patient (2%) died within 30 days after op eration. Symptomatic improvement was achieved in 96% of patients with a mean duration of 22 months. Three- and five-year survivals were 66% and 49%, respectively. In patients with curative resection, the diseas e-free survival at 3 years was 53% (95% CI: 32-86%). The presence of d iffuse hepatic metastases was a predictor of poor survival at 3 years (74% versus 58%; p = 0.05); there was no statistically significant dif ference in survival between functioning and nonfunctioning groups (p > 0.1). Although curative resection for ICC is rare, meaningful palliat ion can be achieved in most patients with rare mortality and acceptabl e morbidity.