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胃腺癌与胃近端息肉病(GAPPS)——一种最近才被描述的罕见胃息肉病综合征——病例报告

Gastric adenocarcinoma and proximal polyposis of the stomach (GAPPS) - a rare recently described gastric polyposis syndrome - report of a case.

作者信息

Beer Andrea, Streubel Berthold, Asari Reza, Dejaco Clemens, Oberhuber Georg

机构信息

Department of Pathology, Medical University of Vienna, Vienna, Austria.

Department of Surgery, Medical University of Vienna, Vienna, Austria.

出版信息

Z Gastroenterol. 2017 Nov;55(11):1131-1134. doi: 10.1055/s-0043-117182. Epub 2017 Nov 15.

Abstract

In rare cases with multiple gastric polyps in the corpus and fundus, a recently described gastric polyposis syndrome called gastric adenocarcinoma and proximal polyposis of the stomach (GAPPS) has to be considered. We report on the findings in a patient fulfilling the criteria of this disease.A female patient born in 1977 underwent gastroscopy in 2005 due to recurrent abdominal pain. Endoscopy revealed more than 100 fundic gland polyps in the corpus and fundus. An ileocolonoscopy was inconspicuous. The patient did not take proton pump inhibitors. In follow-up biopsies, fundic gland polyps with low-grade dysplasia were observed. In 2015 gastroscopy with biopsy revealed for the first time high-grade dysplasia in a polyp, and the patient underwent prophylactic gastrectomy.Macroscopic examination of the gastrectomy specimen revealed hundreds of polyps predominantly measuring 3 mm in diameter covering the fundus and corpus. Histology showed fundic gland polyps, mainly covered by normal appearing foveolae. However, several of them were covered by lesions reminiscent of gastric foveolar adenomas with low- and focally high-grade dysplasia. Molecular pathology revealed a point mutation in the adenomatous polyposis coli promotor 1B. These findings in conjunction with the knowledge that the patient's father had died of gastric carcinoma in his 50 s led to the diagnosis of the autosomal dominant syndrome GAPPS, which has hitherto been described in 9 families.

摘要

在极少数胃体和胃底出现多个胃息肉的病例中,必须考虑一种最近描述的胃息肉病综合征,即胃腺癌和胃近端息肉病(GAPPS)。我们报告了一名符合该疾病标准的患者的检查结果。一名出生于1977年的女性患者因反复腹痛于2005年接受了胃镜检查。内镜检查发现胃体和胃底有100多个胃底腺息肉。回结肠镜检查未见异常。该患者未服用质子泵抑制剂。在后续活检中,观察到有低度异型增生的胃底腺息肉。2015年胃镜检查及活检首次发现一个息肉中有高度异型增生,该患者接受了预防性胃切除术。胃切除标本的宏观检查发现数百个息肉,直径主要为3毫米,覆盖胃底和胃体。组织学显示为胃底腺息肉,主要被外观正常的小凹覆盖。然而,其中一些被类似胃小凹腺瘤的病变覆盖,伴有低度和局灶性高度异型增生。分子病理学显示腺瘤性息肉病大肠杆菌启动子1B存在点突变。这些发现,再加上患者的父亲在50多岁时死于胃癌这一情况,导致诊断为常染色体显性综合征GAPPS,迄今为止该综合征仅在9个家族中被描述过。

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