Marandian M H, Rakhchan M, Mortazavi H
Arch Fr Pediatr. 1981 Aug-Sep;38(7):513-5.
A 7 year-old boy with hypertrophic gastropathy and anemia is described. He was given a substitutive therapy and was under regular control. Upper G.I. bleeding disappeared when he was 15 but hypochlorhydria, radiologic changes and hyperplasia of mucus-secreting cells persisted up to the 22nd year of life. Transient intestinal metaplasia of fundic mucosa was found at 16. Several of these findings are similar to those in Menetrier's disease in adults.
本文描述了一名患有肥厚性胃病和贫血的7岁男孩。他接受了替代疗法并定期接受检查。上消化道出血在他15岁时消失，但胃酸过少、放射学改变和黏液分泌细胞增生一直持续到他22岁。16岁时发现胃底黏膜有短暂的肠化生。这些发现中有几项与成人梅内特里耶病的表现相似。
