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Article
August 1973

Duodenal Wall Tumors and the Zollinger-Ellison SyndromeSurgical Management

Author Affiliations

Milwaukee
From the Division of Surgery, Medical College of Wisconsin, and the Allen-Bradley Medical Science Laboratory, Milwaukee.

Arch Surg. 1973;107(2):334-339. doi:10.1001/archsurg.1973.01350200194040
Abstract

Surgical management of patients with islet-cell, duodenal wall tumors (DWT), and the Zollinger-Ellison syndrome (ZES) is controversial. Complete tumor excision or total gastrectomy has been advocated. Duodenal wall tumors were identified in 13% (103 of 800) of patients in the Z-E Tumor Registry. The characteristics of ZES patients with DWTs and results of surgery were studied. Less than half of the patients with DWTs had solitary lesions. Four subgroups were identified: group 1, 48 patients with localized DWTs; group 2, 26 patients with DWTs and lymph node metastasis; group 3, 24 patients with duodenal wall and pancreatic tumors; and group 4, five patients with DWTs and islet-cell hyperplasia. Total gastrectomy resulted in the best survival when the DWTs were associated with pancreatic or metastatic lesions or both. Attempts at local tumor excision resulted in a 51% ulcer recurrence rate. Local excision of DWTs with less than total gastrectomy was successful in only 20 patients.

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