Pancreatic polypeptide hyperplasia causing watery diarrhea syndrome: a case report.
نویسندگان
چکیده
Neuroendocrine tumours of the pancreas can secrete numerous peptides, leading to various recognizable clinical syndromes. The secretion of pancreatic polypeptide has been used as a marker for neuroendocrine tumours but is considered to be a biologically inert peptide. A 37-year-old woman had watery diarrhea syndrome from pancreatic polypeptide hyperplasia. Only 2 other reported cases in the literature have described pancreatic polypeptide hyperplasia; however, this is the first reported case in which the patient was successfully treated by surgical resection, with a 2-year follow-up. This report and review of the literature illustrate that pancreatic polypeptide hypersecretion may present as a clinical endocrinopathy.
منابع مشابه
[Vasoactive intestinal polypeptide (V.I.P)].
VIPomas can occur as part of the type 1 multiple endocrine neoplasia (MEN) syndrome. VIP is the principal mediator of the watery diarrhea syndrome (also known as pancreatic cholera, Werner-Morrison syndrome, or diarrheogenic islet cell tumor). Watery diarrhea syndrome, with elevated VIP, has also been associated with neurogenic tumors (ganglioneuroma, neuroblastoma, pheochromocytoma), bronchoge...
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Vasoactive intestinal peptideoma (VIPoma) is a rare pancreatic endocrine tumor associated with a well-defined clinical syndrome characterized by watery diarrhea, hypokalemia and metabolic acidosis. In adults, VIPoma is most commonly found in the pancreas, with 80% of the tumors occurring in the body and tail and 20% occurring in the pancreatic head. VIPomas can represent a significant diagnosti...
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عنوان ژورنال:
- Canadian journal of surgery. Journal canadien de chirurgie
دوره 42 1 شماره
صفحات -
تاریخ انتشار 1999