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Submitted on October 11, 2007
Accepted on January 31, 2008
Digestive Diseases Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland; Division of Digestive and Liver Diseases, University "La Sapienza", Rome, Italy; Department of Pathology and Laboratory Medicine, Section of Anatomic Pathology, University of Parma, Parma, Italy; Department for Internal Medicine I, University Hospital Hamburg-Eppendorf, Hamburg, Germany: Department of Medicine and Bio-regulatory Science, Graduate School of Medical Science, Kyushu University, Fukuoka, Japan; and Biostatistics and Data Management Section, National Cancer Institute, National Institutes of Health, Bethesda, Maryland
* To whom correspondence should be addressed. E-mail: RobertJ{at}bdg10.niddk.nih.gov.
Context: Multiple Endocrine Neoplasia-Type I(MEN1) patients frequently develop Zollinger-Ellison Syndrome(ZES). These patients can develop proliferative changes of gastric ECL-cells and gastric carcinoids(ECL-cell tumors). ECL-cell changes have been extensively studied in sporadic ZES patients and can be precursor lesions of gastric carcinoids, but little is known about factors influencing their severity or development of carcinoids in MEN1/ZES patients.
Objectives: To prospectively analyze ECL-cell changes and gastric carcinoids (ECL-cell tumors) in a large series of MEN1/ZES patients to detect risk factors and deduct clinical guidelines.
Setting: Prospective study at two tertiary-care research centers.
Patients: Fifty-seven consecutive MEN1/ZES patients.
Interventions and Outcome Measures: Assessment of MEN1, gastric hypersecretion and gastroscopy with multiple biopsies according to a fixed protocol and tumor status. ECL-cell changes and
-hCG staining were assessed in each biopsy and correlated with clinical, laboratory and MEN1 features.
Results: ECL-cell proliferative changes were universally present, advanced changes in 53% and carcinoids in 23%. Gastric nodules are common and are frequently associated with carcinoids. Patients with high fasting serum gastrin levels, long disease-duration or a strong
-hCG staining in a biopsy are at higher risk for an advanced ECL-cell lesion and/or gastric carcinoid.
Conclusions: Gastric carcinoids and/or advanced ECL-cell changes are frequent in MEN1/ZES patients and therefore regular surveillance gastroscopy with multiple routine biopsies and biopsies of all mucosal lesions are essential. Clinical/laboratory data and biopsy results can be used to identify a subgroup of MEN1/ZES patients with a significantly increased risk for developing gastric carcinoids allowing development of better surveillance strategies.
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