Gastric epithelial neoplasm of fundic-gland mucosa lineage: proposal for a new classification in association with gastric adenocarcinoma of fundic-gland type.
Gastric epithelial neoplasm of fundic-gland mucosa lineage: proposal for a new classification in association with gastric adenocarcinoma of fundic-gland type.
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胃底腺粘膜系上皮性肿瘤:与胃底腺型胃腺癌相关的新分类建议。
DOI:
10.1007/s00535-021-01813-z
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发表时间:
2021-09
影响因子:
6.3
通讯作者:
Nagahara A
中科院分区:
文献类型:
--
作者:
Ueyama H;Yao T;Akazawa Y;Hayashi T;Kurahara K;Oshiro Y;Yamada M;Oda I;Fujioka S;Kusumoto C;Fukuda M;Uchita K;Kadota T;Oono Y;Okamoto K;Murakami K;Matsuo Y;Kato M;Maehata T;Yahagi N;Yasuhara Y;Yada T;Uraushihara K;Yamane T;Matsuo T;Ito M;Maruyama Y;Osako A;Ono S;Kato M;Yagi K;Hashimoto T;Tomita N;Tsuyama S;Saito T;Matsumoto K;Matsumoto K;Watanabe S;Uemura N;Chiba T;Nagahara A
Gastric adenocarcinoma of fundic-gland type (GA-FG) is a rare variant of gastric neoplasia. However, the etiology, classification, and clinicopathological features of gastric epithelial neoplasm of fundic-gland mucosa lineage (GEN-FGML; generic term of GA-FG related neoplasm) are not fully elucidated. We performed a large, multicenter, retrospective study to establish a new classification and clarify the clinicopathological features of GEN-FGML. One hundred GEN-FGML lesions in 94 patients were collected from 35 institutions between 2008 and 2019. We designed a new histopathological classification of GEN-FGML using immunohistochemical analysis and analyzed via clinicopathological, immunohistochemical, and genetic evaluation. GEN-FGML was classified into 3 major types; oxyntic gland adenoma (OGA), GA-FG, and gastric adenocarcinoma of fundic-gland mucosa type (GA-FGM). In addition, GA-FGM was classified into 3 subtypes; Type 1 (organized with exposure type), Type 2 (disorganized with exposure type), and Type 3 (disorganized with non-exposure type). OGA and GA-FG demonstrated low-grade epithelial neoplasm, and GA-FGM should be categorized as an aggressive variant of GEN-FGML that demonstrated high-grade epithelial neoplasm (Type 2 > 1, 3). The frequent presence of GNAS mutation was a characteristic genetic feature of GEN-FGML (7/34, 20.6%; OGA 1/3, 33.3%; GA-FG 3/24, 12.5%; GA-FGM 3/7, 42.9%) in mutation analysis using next-generation sequencing. We have established a new histopathological classification of GEN-FGML and propose a new lineage of gastric epithelial neoplasm that harbors recurrent GNAS mutation. This classification will be useful to estimate the malignant potential of GEN-FGML and establish an appropriate standard therapeutic approach. The online version contains supplementary material available at 10.1007/s00535-021-01813-z.
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Park ES;Kim YE;Park CK;Yao T;Kushima R;Kim KM
通讯作者:
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