Menetrier氏病是一种少见的疾病,在国内文献中仅见三例报告。最近,我们发现一例典型的Menetrier氏病。兹将该病例的临床病理资料整理,报告如下: 一、临床病史患者周××,男,40岁,公社社员。因上腹疼痛8年,腹泻7年,加剧半年于1978年6月4日入院。患者从70年开始出现饭后上腹部胀痛,71年起伴有腹泻,为粘液白冻样大便,有时为脂肪样,每日2—4次。春冬季发作频繁。75年经药物治疗(用药不详),症状有所改善。近年来饭后腹部疼痛加剧。无呕吐、呕血、黑便。间歇发生浮肿已1年余,多在下 Menetrier’s disease is a rare disease and only three cases have been reported in domestic literature. Recently, we found a typical case of Menetrier’s disease. The clinicopathological data of this case are then collated and reported as follows: I. Clinical history Patient Zhou X, male, 40 years old, Commune member. Due to 8 years of epigastric pain and 7 years of diarrhea, she was admitted to hospital on June 4, 1978 in an intensified half year. From the 70th year onwards, the patient developed upper abdominal pain after a meal and 71 years had diarrhea. It was mucous white, cold-like stool, sometimes fat-like, 2-4 times a day. Spring and winter attacks are frequent. After 75 years of drug treatment (drugs are unknown), the symptoms have improved. In recent years, abdominal pain has worsened after a meal. No vomiting, vomiting, black stools. Intermittent edema has been more than 1 year, mostly under