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Yale Surgery |
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330 Cedar Street
FMB 102
New Haven, CT
06520-8062 |
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(203) 785-2697 Tel.
(203) 737-2116 Fax
E-mail |
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Pancreatic Surgery
Pancreatic Endocrine Diseases (Neuroendocrine pancreatic tumors)
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Islet cell tumors |
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Gastrinoma |
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Zollinger-Ellison Syndrome |
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Insulinoma |
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Glucagonoma |
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Somatostatinoma |
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VIPoma |
The Pancreas
The pancreas is an oblong gland about 6 - 8 inches in length, which lies
beneath the stomach. The pancreas has two separate functions: the exocrine
portion (about 80% of the gland) which secretes enzymes important for
the digestion of food, and the endocrine portion which secretes several
hormones including insulin, glucagon, somatostatin, pancreatic polypeptide
and other.
Pancreatic Endocrine Tumors
Any of the cells which secrete hormones may be transformed into a tumor
which over-secretes the hormone. The tumors are named based on the hormone
they produce, such as glucagonoma, insulinoma, gastrinoma, and somatostatinoma.
These tumors can produce a wide range of symptoms related to the excessive
hormone production. Endocrine pancreatic tumors may also be non-functioning.
Occasionally, these tumors are inherited with other tumors in the Multiple
Endocrine Neoplasia (MEN) type 1 syndrome. Most pancreatic endocrine tumors
require surgical resection. Not all neuroendocrine tumors are malignant.
Pancreatic Cancer (Adenocarcinoma)
Pancreatic cancer is more common than the neuroendocrine tumors, and arises
from the exocrine portion of the pancreas. This is a different entity
than the pancreatic endocrine tumors and carries a worse prognosis. Its
treatment often involves surgery and chemo-radiation.
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