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在19年的随访期间,起源于异位胃腺的胃底腺型腺癌。

Gastric adenocarcinoma of fundic gland type arising from heterotopic gastric glands during a 19-year follow-up period.

作者信息

Uozumi Takeshi, Seki Hideyuki, Matsuzono Emi, Sogabe Susumu, Sugai Nozomu, Fujita Jun, Suzuki Junichi, Akimoto Mayuko, Yanai Mitsuru, Suzuki Akira

机构信息

Departments of Gastroenterology, KKR Sapporo Medical Center, 6-3-40, Hiragishi 1jou, Toyohira-ku, Sapporo, Hokkaido, 062-0931, Japan.

Department of Pathology, KKR Sapporo Medical Center, Sapporo, Japan.

出版信息

Clin J Gastroenterol. 2019 Dec;12(6):556-561. doi: 10.1007/s12328-019-00989-5. Epub 2019 Jun 4.

Abstract

A 73-year-old man with prior history of duodenal ulcer has been undergoing periodic upper gastrointestinal endoscopy since 1999. In 2017, a 25-mm submucosal tumor-like protrusion was detected in the lesser curvature of the upper stomach; histological examination of the lesion revealed gastric adenocarcinoma of fundic gland type. En bloc resection was achieved using endoscopic submucosal dissection. The patient was histopathologically diagnosed with gastric adenocarcinoma of fundic gland type arising from heterotopic gastric glands. Immunohistochemical staining was positive for MUC5AC, MUC6, pepsinogen I, and proton pump but negative for MUC2 and CD10. Moreover, the patient's Ki-67 labeling index score was extremely low. The presence of MUC5AC indicated that the tumor differentiated to the foveolar epithelium and fundic glands. Gastric adenocarcinoma of fundic gland type that differentiates to several directions has a higher malignant potential than the disease that differentiates to chief cells. A retrospective review of the patient's previous endoscopic examination revealed that the submucosal tumor-like protrusion existed since 2000; tumor size increased from 8 mm in 2000 to 25 mm in 2017. The present case is rare in that the carcinoma arose from heterotopic gastric glands. Moreover, the 19-year follow-up revealed that the tumor differentiated to the foveolar epithelium, considered as having high-grade malignancy.

摘要

一名73岁男性,有十二指肠溃疡病史,自1999年以来一直在接受定期上消化道内镜检查。2017年,在上胃部小弯侧发现一个25毫米的黏膜下肿瘤样隆起;对该病变进行组织学检查,结果显示为胃底腺型胃癌。采用内镜黏膜下剥离术实现了整块切除。患者经组织病理学诊断为异位胃腺引起的胃底腺型胃癌。免疫组织化学染色显示MUC5AC、MUC6、胃蛋白酶原I和质子泵呈阳性,但MUC2和CD10呈阴性。此外,患者的Ki-67标记指数评分极低。MUC5AC的存在表明肿瘤分化为小凹上皮和胃底腺。向多个方向分化的胃底腺型胃癌比向主细胞分化的疾病具有更高的恶性潜能。对患者之前的内镜检查进行回顾发现,黏膜下肿瘤样隆起自2000年就已存在;肿瘤大小从2000年的8毫米增加到2017年的25毫米。本例罕见之处在于癌起源于异位胃腺。此外,19年的随访显示肿瘤分化为小凹上皮,被认为具有高度恶性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d66/6892357/da91bc8f821d/12328_2019_989_Fig1_HTML.jpg

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