Shibagaki Kotaro, Kushima Ryoji, Sekine Shigeki, Mishiro Tsuyoshi, Kotani Satoshi, Miyaoka Yoichi, Ishimura Norihisa, Araki Asuka, Ohnuma Hideyuki, Niino Daisuke, Ishihara Shunji
Department of Endoscopy, Shimane University Hospital, Shimane, Japan.
Department of Pathology, Shiga University of Medical Science, Shiga, Japan.
Dig Endosc. 2025 Jun;37(6):611-628. doi: 10.1111/den.14980. Epub 2025 Jan 22.
Chronic Helicobacter pylori (Hp) infection is the largest etiological factor for gastric cancer, but in recent years the reports of Hp-naïve gastric neoplasms (HpNGNs) have increased as the Hp-infected population in Japan has been declining. The histopathologic spectrum of HpNGNs differs significantly from that of conventional Hp-infected gastric neoplasms. Molecularly, the former harbor considerably fewer genetic and epigenetic abnormalities, reflecting the absence of chronic inflammatory conditions in the gastric mucosa. The majority of HpNGNs fall within several specific histological entities; each arise from particular background mucosa. Most originate from the fundic gland mucosa and have a gastric immunophenotype, as seen in foveolar-type gastric adenoma (FGA), oxyntic gland adenoma (OGA)/gastric adenocarcinoma of fundic gland type (GA-FG), signet-ring cell carcinoma (SRCC), and sporadic fundic gland polyp with dysplasia (FGPD). In contrast, tumors arising from the pyloric or cardiac gland mucosa have a diverse immunophenotype, as seen in intestinal-type gastric dysplasia (IGD) and gastric cardiac carcinoma. FGA, FGPD, SRCC, and IGD are mostly found as small intramucosal lesions. OGA/GA-FG frequently progresses to invasive carcinoma, but only a few have lymph node metastases. Thus, these tumors are regarded as precancerous lesions by Western pathologists, while in Japan they tend to be diagnosed as carcinomas, even in cases of low-grade dysplasia. Gastric cardiac carcinomas, on the other hand, are often found as advanced carcinomas and harbor a high malignant biological potential. A new diagnostic framework for gastric neoplasms is required in the present era of Hp-naïve individuals in Japan.
慢性幽门螺杆菌(Hp)感染是胃癌的最大病因,但近年来,随着日本Hp感染人群的减少,未感染Hp的胃肿瘤(HpNGNs)报告有所增加。HpNGNs的组织病理学谱与传统Hp感染的胃肿瘤有显著差异。在分子层面,前者的基因和表观遗传异常要少得多,这反映出胃黏膜中不存在慢性炎症。大多数HpNGNs属于几种特定的组织学类型;每种类型都起源于特定的背景黏膜。大多数起源于胃底腺黏膜,具有胃免疫表型,如见于胃小凹型胃腺瘤(FGA)、胃泌酸腺腺瘤(OGA)/胃底腺型胃癌(GA-FG)、印戒细胞癌(SRCC)和伴有发育异常的散发性胃底腺息肉(FGPD)。相比之下,起源于幽门腺或贲门腺黏膜的肿瘤具有多样的免疫表型,如见于肠型胃发育异常(IGD)和胃贲门癌。FGA、FGPD、SRCC和IGD大多表现为小的黏膜内病变。OGA/GA-FG常进展为浸润性癌,但只有少数有淋巴结转移。因此,这些肿瘤被西方病理学家视为癌前病变,而在日本,即使是低级别发育异常的病例也往往被诊断为癌。另一方面,胃贲门癌常表现为进展期癌,具有较高的恶性生物学潜能。在日本目前未感染Hp个体的时代,需要一个新的胃肿瘤诊断框架。