Home » AGEB Journal » Issues » Volume 81" » Fasc.3 - Letters » Article details

An unusual cause of anemia : familial hyperplastic gastric polyposis

Journal Volume 81 - 2018
Issue Fasc.3 - Letters
Author(s) S. Köklü, G. Guler
Full article
Full Article
VIEW FREE PDF
(1) Professor of Gastroenterology, Ortadogu 19 Mayis Hospital, Dikmen, Cankaya, Ankara, Turkey ; (2) Professor of Pathology, Hekim Center, Cankaya, Ankara, Turkey.

Familial hyperplastic gastric polyposis is a very rare entity, and up to now, only few cases have been reported (1, 2). A 57-year-old man was admitted with complaints of dyspepsia for a long time. He was taking proton pump inhibitors for about 30 years. His family history revealed gastric polyposis in his father and brother; however, there was no history of gastrointestinal cancer. Physical examination was unremarkable. On admission, laboratory studies were normal other than a hemoglobin level of 10.2 g/dL. Upper endoscopic examination revealed dozens of polyps (3-12 mm in diameter) through out the fundus and corpus of the stomach (Fig. 1). Larger polyps were removed by cutting with snare. Histological examination of the materials was compatible with hyperplastic polyps (Fig. 2). Helicobacter Pylori was positive at antrum biopsy. Since past medical history of our patient revealed standard treatment against Helicobacter Pylori for several times, he was prescribed sequential therapy for eradication. The patient refused to perform colonoscopic examination and further genetic analysis.

© Acta Gastro-Enterologica Belgica.
PMID 30350540