November 1967

Carcinoid Syndrome Associated With Pancreatic Tumors

Author Affiliations

New York

From the Division of Experimental Chemotherapy, Sloan-Kettering Institute for Cancer Research, and the departments of medicine and pathology, Memorial Hospital for Cancer and Allied Diseases, and the James Ewing Hospital, New York.

Arch Intern Med. 1967;120(5):575-580. doi:10.1001/archinte.1967.00300040059010

CARCINOID tumors may originate from the stomach, duodenum, small and large intestines, and rectum, since the Kultschitzky, or argentaffin cell, from which carcinoid tumors are derived, is found in all these areas. Since these cells are also found in the gallbladder and pancreatic ducts, it is not surprising that functioning carcinoid tumors have been reported from these locations.1-3 Several recent reports have described patients with a variety of pancreatic neoplasms, not of argentaffin cell origin, who nevertheless had typical carcinoid syndromes, including elevated urinary levels of the serotonin metabolite, 5-hydroxyindoleacetic acid (5-HIAA). These tumors have included adenocarcinoma of the pancreas 4-7 and islet cell carcinoma.8-10 The latter two reports9,10 described patients with hypoglycemia as well as the carcinoid syndrome.

The present study describes a patient with metastatic islet cell carcinoma who had the manifestations of the carcinoid syndrome, including cutaneous telangiectasis, diarrhea, persistently increased skin pigmentation, a hyperkinetic

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