Cystic Glucagonoma: A Rare Variant of an Uncommon Neuroendocrine Pancreas Tumor

Kimberly Brown, Theresa Kristopaitis, Sherri Yong, Gregorio Chejfec, Jack Pickleman

Research output: Contribution to journalArticle

21 Scopus citations

Abstract

Glucagon-producing neuroendocrine tumors typically present with a characteristic constellation of symptoms including necrolytic migratory erythema, non-insulin-dependent diabetes, weight loss, anemia, glossitis, and an increased thrombotic tendency. Most glucagonomas are solid and arise in the body or tail of the pancreas. We report two cases of cystic glucagonoma, one found incidentally in an asymptomatic patient and one in a patient with weight loss and diabetes but no rash. In the first patient, distal pancreatectomy and splenectomy were curative, whereas the second patient continued to exhibit elevated serum glucagon levels and symptoms of glucose intolerance in the absence of demonstrable metastases. Cystic glucagonoma is a unique variant of classic glucagonoma and should be considered in the differential diagnosis of cystic pancreatic neoplasms.

Original languageEnglish (US)
Pages (from-to)533-536
Number of pages4
JournalJournal of Gastrointestinal Surgery
Volume2
Issue number6
StatePublished - Nov 1998
Externally publishedYes

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Keywords

  • Cystic pancreatic neoplasm
  • Glucagonoma

ASJC Scopus subject areas

  • Surgery

Cite this

Brown, K., Kristopaitis, T., Yong, S., Chejfec, G., & Pickleman, J. (1998). Cystic Glucagonoma: A Rare Variant of an Uncommon Neuroendocrine Pancreas Tumor. Journal of Gastrointestinal Surgery, 2(6), 533-536.