Gastric adenocarcinoma with enteroblastic differentiation.

IF 3.5 4区 医学 Q3 CELL BIOLOGY
Pathobiology Pub Date : 2025-01-07 DOI:10.1159/000543330
Ádám Ferenczi, Levente Kuthi, Anita Sejben
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引用次数: 0

Abstract

Introduction: Gastric adenocarcinoma with enteroblastic differentiation (GAED) is a rare entity with worse prognosis compared to conventional gastric adenocarcinomas. Its histological characteristics are fetal gut-like architecture and tumor cells with cytoplasmic clearing, as well as positive immunohistochemical reaction to at least one of the enteroblastic markers. Hereby, we present a case of GAED with neuroendocrine marker positivity, with whole exome sequencing (WES), and an updated literature review.

Case presentation: A 68-year-old woman presented with abdominal pain. Gastric wall thickening raised suspicion of gastric cancer, thus gastroscopy was performed, and biopsy samples were taken, which confirmed malignancy. Neoadjuvant systemic chemotherapy was initiated, and total gastrectomy was performed. Microscopically, pleomorphic polygonal cells were visible with clear cytoplasm and high grade cellular atypia. Alcian blue and PAS stains demonstrated positivity for acidic and neutral mucins. P53 IHC was negative, indicative of null-phenotype, while Syntaxin-1 and Chromogranin showed focal positivity. SALL4 and Glypican 3 were positive, however, AFP displayed only minimal, uncertain positivity. The Ki67 labeling index was 70%. Due to the morphological and immunohistochemical characteristics, the tumor was concluded as GAED with neuroendocrine marker positivity. WES was carried out revealing 4 pathogenic, including TP53, KLHL7, RAPSN, and ACTA1, and 3 likely pathogenic mutations, encompassing PNKP, HNF1A, and ADNP.

Discussion: GAED is a rare subtype of gastric adenocarcinomas, representing 0.3-5.4% of all cases and has an unclarified etiology. Our WES results identified new pathogenic and likely pathogenic mutations. From a differential diagnostic point of view, hepatoid adenocarcinoma, and the possibility of metastatic origin has to be excluded.

胃腺癌伴肠母细胞分化。
摘要胃腺癌伴肠母细胞分化(GAED)是一种罕见的疾病,其预后较常规胃腺癌差。其组织学特征为胎儿肠样结构和细胞质清除的肿瘤细胞,以及对至少一种肠母细胞标志物的免疫组化反应阳性。在此,我们报告一例神经内分泌标志物阳性的GAED病例,采用全外显子组测序(WES),并进行最新的文献综述。病例介绍:68岁女性,腹痛。胃壁增厚提示胃癌,行胃镜检查,活检证实为恶性。开始新辅助全身化疗,并行全胃切除术。镜下可见多形性多角形细胞,细胞质清晰,细胞高度异型性。阿利新蓝染色和PAS染色显示酸性和中性粘蛋白阳性。P53 IHC呈阴性,提示为零表型,而Syntaxin-1和Chromogranin呈局灶性阳性。SALL4和Glypican 3为阳性,而AFP仅表现出微小的、不确定的阳性。Ki67标记指数为70%。根据形态学和免疫组织化学特征,结论为GAED,神经内分泌标志物阳性。WES揭示了4种致病突变,包括TP53、KLHL7、RAPSN和ACTA1,以及3种可能的致病突变,包括PNKP、HNF1A和ADNP。讨论:GAED是一种罕见的胃腺癌亚型,占所有病例的0.3-5.4%,病因不明。我们的WES结果发现了新的致病突变和可能的致病突变。从鉴别诊断的角度来看,肝样腺癌和转移起源的可能性必须排除。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Pathobiology
Pathobiology 医学-病理学
CiteScore
8.50
自引率
0.00%
发文量
47
审稿时长
>12 weeks
期刊介绍: ''Pathobiology'' offers a valuable platform for the publication of high-quality original research into the mechanisms underlying human disease. Aiming to serve as a bridge between basic biomedical research and clinical medicine, the journal welcomes articles from scientific areas such as pathology, oncology, anatomy, virology, internal medicine, surgery, cell and molecular biology, and immunology. Published bimonthly, ''Pathobiology'' features original research papers and reviews on translational research. The journal offers the possibility to publish proceedings of meetings dedicated to one particular topic.
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