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Pancreatic polypeptide hyperplasia causing watery diarrhea syndrome: a case report.

Abstract
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.
AuthorsJ L Pasieka, N Hershfield
JournalCanadian journal of surgery. Journal canadien de chirurgie (Can J Surg) Vol. 42 Issue 1 Pg. 55-8 (Feb 1999) ISSN: 0008-428X [Print] Canada
PMID10071589 (Publication Type: Case Reports, Journal Article, Review)
Chemical References
  • Pancreatic Polypeptide
Topics
  • Adult
  • Diagnosis, Differential
  • Female
  • Humans
  • Hyperplasia
  • Islets of Langerhans (pathology)
  • Pancreatectomy
  • Pancreatic Neoplasms (diagnosis, pathology, surgery)
  • Pancreatic Polypeptide (blood)
  • Vipoma (diagnosis, pathology, surgery)

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