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March 17, 1962

Peptic Ulcer as a Manifestation of Familial Polyendocrine Disease: Report of Two Cases Occurring in Sisters, with a Preliminary Report of Eight Other Family Members

Author Affiliations

Detroit

From the departments of internal medicine and pathology, Henry Ford Hospital, Detroit, and the Department of Internal Medicine, Manhattan Veterans Administration Hospital, New York City (Dr. Ballard).

JAMA. 1962;179(11):854-858. doi:10.1001/jama.1962.03050110022004
Abstract

Two cases of polyendocrine disease occurring in sisters and presenting as intractable peptic ulcer are reported. In both cases the criteria of the Zollinger-Ellison syndrome were satisfied. One sister, aged 53, after a course of recurrent ulcer and perforation of the jejunum, died in renal failure caused by nephrocalcinosis. Abnormalities were found in the pituitary, parathyroids, pancreas, and adrenals. The other sister, aged 46, had intractable ulcer symptoms. Surgical findings indicated polyendocrine disease. She became virtually symptom-free after subtotal gastrectomy and removal of 3 pancreatic tumors. Eight other members of the family have been similarly affected. The authors believe that the Zollinger-Ellison syndrome is an expression of polyendocrine disease.

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