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Metastatic pancreatic neuroendocrine carcinoma causing Cushing's syndrome. ACTH secretion by metastases 3 years after resection of nonfunctioning primary cancer.

AbstractCONCLUSION:
Following resection of a nonfunctioning neuroendocrine carcinoma of the pancreas, subsequent metastases, in the absence of a primary cancer (resected), developed the capacity to secrete ACTH and create the Cushing syndrome.
BACKGROUND:
Although neuroendocrine carcinomas of the pancreas may produce one or more hormones and may switch secretion to a different hormone, no report is identified of a metastasis, in the absence of the primary tumor, developing de novo the capacity to secrete ACTH.
METHODS:
A nonfunctioning islet cell carcinoma was resected and immunochemically stained for multiple hormones. Three years later hepatic metastases were partially resected and stained as before.
RESULTS:
The primary cancer stained negative for ACTH and cortisol, positive for serotonin, and focally positive for gastrin. Three years later, after the development of a florid Cushing syndrome, the metastasis stained strongly for ACTH and negative for serotonin.
AuthorsL Zhu, D R Domenico, J M Howard
JournalInternational journal of pancreatology : official journal of the International Association of Pancreatology (Int J Pancreatol) Vol. 19 Issue 3 Pg. 205-8 (Jun 1996) ISSN: 0169-4197 [Print] United States
PMID8807366 (Publication Type: Case Reports, Journal Article)
Chemical References
  • Serotonin
  • Adrenocorticotropic Hormone
Topics
  • Adrenocorticotropic Hormone (metabolism)
  • Carcinoma, Neuroendocrine (complications, metabolism, secondary)
  • Cushing Syndrome (etiology)
  • Humans
  • Immunohistochemistry (methods)
  • Male
  • Middle Aged
  • Pancreatic Neoplasms (complications, metabolism, secondary)
  • Serotonin (metabolism)
  • Staining and Labeling

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