Department of Pathology, Affiliated Hospital of Zunyi Medical University, Guizhou, 563003, China.
Diagn Pathol. 2020 Oct 23;15(1):131. doi: 10.1186/s13000-020-01047-2.
Gastric adenocarcinoma of the fundic gland type (GA-FG) has been added to the 2019 edition of the World Health Organization's list of digestive system-associated cancers. This lesion differentiates toward the fundic gland and mostly involves chief cell-predominant differentiation with low-grade cytology. Clinicians and pathologists are still unaware of this rare disease; consequently, some cases are incorrectly diagnosed. This study aimed to investigate the clinicopathological features of GA-FG using retrospective analyses of endoscopic and pathological findings.
Samples were collected from patients diagnosed with GA-FG. The clinical courses of all patients were monitored prospectively and reviewed retrospectively. Available clinical information, endoscopic features, pathological appearance, and follow-up data were assessed. Immunohistochemistry [mucin (MUC) 2, MUC5, MUC6, P53, CDX2, Ki67, SYN, CD56, CGA, β-catenin, and pepsinogen-I] was examined using Envision two-step method.
Eight cases of endoscopic submucosal dissection (ESD) were obtained from our institution. Patient age ranged from 48 to 80 years (mean, 65 years). Some patients were on acid-suppressing medication. Most lesions were located in the upper third (n = 7) and one was in the middle third of the stomach. Six lesions were of the superficial flat type, whereas two were of the superficial elevated type. Narrow-band imaging using magnifying endoscopy showed irregular microvascular patterns (MVPs) in four cases and regular MVPs in the remaining cases. All lesions were primarily solitary and ~ 6 mm in diameter (largest, 12 mm). The main body of the tumors were localized in the mucosal layer, of which six cases invade into the submucosal layer. Well-formed glands of chief cells were predominant. Tumor cells were positive for pepsinogen-I, MUC6, SYN, and CD56. Lymphatic and vascular infiltration and metastatic and recurrent disease were not observed in any case.
GA-FG, a well-differentiated adenocarcinoma with mild atypia, can be completely removed using ESD, with a favorable prognosis in patients.
胃底腺型腺癌(GA-FG)已被纳入 2019 年版世界卫生组织消化系统相关癌症清单。这种病变向胃底腺分化,主要表现为以主细胞为主的低级别细胞学分化。临床医生和病理学家仍然不了解这种罕见的疾病;因此,一些病例被误诊。本研究旨在通过回顾性分析内镜和病理检查结果,探讨 GA-FG 的临床病理特征。
收集诊断为 GA-FG 的患者样本。前瞻性监测所有患者的临床病程,并进行回顾性分析。评估了可用的临床信息、内镜特征、病理表现和随访数据。采用 Envision 两步法进行免疫组织化学(黏蛋白[MUC]2、MUC5、MUC6、P53、CDX2、Ki67、SYN、CD56、CGA、β-连环蛋白和胃蛋白酶原-I)检查。
从我院获得 8 例内镜黏膜下剥离术(ESD)标本。患者年龄 48 至 80 岁(平均 65 岁)。部分患者正在服用抑酸药物。大多数病变位于上 1/3(n=7),1 例位于胃中 1/3。6 例病变为浅表平坦型,2 例为浅表隆起型。窄带成像放大内镜显示 4 例不规则微血管模式(MVP)和其余 4 例规则 MVP。所有病变均为单发,直径约 6mm(最大直径 12mm)。肿瘤主体局限于黏膜层,其中 6 例侵犯黏膜下层。主要由主细胞形成的腺体为主。肿瘤细胞对胃蛋白酶原-I、MUC6、SYN 和 CD56 呈阳性。未观察到任何病例存在淋巴管和血管浸润、转移和复发。
GA-FG 是一种分化良好的、轻度异型性的腺癌,可通过 ESD 完全切除,患者预后良好。