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In 1947, a patient with metastatic isletcelltumor was treated for intractable ulcer disease at the University of Chicago Medical Center.
2
We report three cases of cystic isletcelltumors, two caused by gastrinomas and the other by an islet cell carcinoma.
3
Overall survival was 61% and 35% at 5 and 10 years, respectively, with no difference between carcinoid and isletcelltumors.
4
A retrospective review at our tertiary referral center (from 1976 to 1999) identified 27 patients with primary duodenal carcinoid lesions, excluding functional isletcelltumors.
1
Pancreaticendocrineneoplasms (PENs) are rare tumors, and little is known about their genetic and chromosomal alterations.
2
One patient had a ductal adenocarcinoma, two presented with pancreaticendocrineneoplasms and the last one had an intraductal papillary mucinous neoplasia.
3
We discuss the diagnosis of pancreatic ductal adenocarcinoma and of other pancreatic epithelioid tumors including pancreaticendocrineneoplasms, solid pseudopapillary tumors, and acinar cell carcinomas.
1
Pancreaticneuroendocrineneoplasms (PanNENs) have an unpredictable clinical course that varies from indolent to highly malignant.
2
Methods: We examined a prospectively maintained, single-institution database to identify patients who underwent potentially curative resection of non-metastatic primary pancreaticneuroendocrineneoplasms.
Translations for malignant pancreatic endocrine tumor