On the origin of gastric tumours: analysis of a case with intramucosal gastric carcinoma and oxyntic gland adenoma
On the origin of gastric tumours: analysis of a case with intramucosal gastric carcinoma and oxyntic gland adenoma
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论胃肿瘤的起源:粘膜内胃癌合并泌酸腺瘤一例分析
DOI:
10.1002/path.6050
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发表时间:
2023
期刊:
影响因子:
--
通讯作者:
Seno Hiroshi
中科院分区:
文献类型:
--
作者:
Kumagai Ken;Shimizu Takahiro;Nikaido Mitsuhiro;Hirano Tomonori;Kakiuchi Nobuyuki;Takeuchi Yasuhide;Minamiguchi Sachiko;Sakurai Takaki;Teramura Mari;Utsumi Takahiro;Hiramatsu Yukiko;Nakanishi Yuki;Takai Atsushi;Miyamoto Shin'ichi;Ogawa Seishi;Seno Hiroshi
Most gastric cancers develop in inflamed gastric mucosa due toHelicobacter pyloriinfection, typically with metaplastic changes. However, the origins of gastric cancer remain unknown. Here, we present a case of intramucosal gastric carcinoma (IGC) and oxyntic gland adenoma (OGA) derived from spasmolytic polypeptide‐expressing metaplasia (SPEM). Early gastric cancer adjacent to a polyp was found in the upper corpus of a 71‐year‐old woman withoutH. pyloriinfection and was endoscopically resected. Histological examination showed IGC and OGA, both of which had predominant MUC6 expression. Interestingly, gastric glands with enriched MUC6‐positive mucous cells, referred to as SPEM, expanded between them. Whole‐exome sequencing analysis revealed a truncatingKRAS(G12D) mutation in IGC, OGA, and SPEM. In addition,TP53andCDKN2Amutations and a loss of chromosome 17p were found in the IGC, whereas aGNASmutation was observed in the OGA. These results indicated that IGC and OGA originated from theKRAS‐mutated SPEM. © 2023 The Pathological Society of Great Britain and Ireland.