Gastric adenocarcinoma with enteroblastic differentiation: Lessons from a rare case

Kunihiko Takahashi, Masaya Yokoyama, Junji Kita, Nobuo Hirayama, Kentaro Chochi, Aya Nakagawa, Mayuko Kinoshita, Hiroe Toyoda, M. Furihata, T. Furihata, Keiji Sano, Hisahiro Matsubara
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Abstract

Gastric adenocarcinoma with enteroblastic differentiation (GAED), also known as clear cell carcinoma or fetal gut-like adenocarcinoma is a special type of adenocarcinoma characterized by primitive intestine-like structures. GAED partially overlaps with alfa-fetoprotein (AFP)-producing gastric carcinoma (APGC). There is insufficient information on the biological behavior of GAED, which has a worse prognosis compared to conventional gastric carcinoma (GC). We introduce an 82-year-old man who presented 4 years ago with severe epigastralgia; the patient then underwent distal gastrectomy for a large GC. The patient was initially diagnosed with well-to-moderately differentiated gastric adenocarcinoma with lymphatic invasion and without nodal involvement, resulting in a TNM classification of T1N0M0, stage IB. Follow-up computed tomography (CT) 31 months after the gastrectomy revealed a hepatic lesion. Lateral segmentectomy of the liver was performed for therapeutic diagnosis. Pathology specimens from the resected tissue were characterized by glycogen-rich neoplastic cells with eosinophilic cytoplasm with a focal glandular component on hematoxylin-eosin staining and periodic acid-Schiff staining. By retrospective analysis using immunohistochemical staining, Glypican 3 was partially positive and spalt-like transcription factor 4 (SALL-4) was strongly positive in the resected GC and metastatic hepatic carcinoma, indicating that GAED metastasized to the liver. Although exceedingly rare, surgeons should recognize GAED as one of the special types of GC. Treatment guidelines for GAED have not yet been established; however, pathological confirmation of GAED when encountering an APGC by immunohistochemical staining for Glypican 3 and SALL-4 is essential to recognize its malignant biological behavior unlike conventional GC.
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具有肠细胞分化的胃腺癌:一个罕见病例的启示
有肠细胞分化的胃腺癌(GAED),又称透明细胞癌或胎儿肠样腺癌,是一种特殊类型的腺癌,其特征是原始肠样结构。GAED 与产生甲胎蛋白(AFP)的胃癌(APGC)部分重叠。与传统胃癌(GC)相比,GAED的预后较差,目前有关GAED生物学行为的信息尚不充分。 我们介绍了一名 82 岁的男性患者,他在 4 年前因严重上腹痛而就诊,随后因巨大的 GC 而接受了远端胃切除术。患者最初被诊断为淋巴管浸润的好中分化胃腺癌,无结节受累,TNM分级为T1N0M0,IB期。胃切除术后 31 个月的随访计算机断层扫描(CT)显示有肝脏病变。为进行治疗诊断,患者接受了肝脏侧段切除术。切除组织的病理标本经苏木精-伊红染色和周期性酸-Schiff染色,可见富含糖原的肿瘤细胞,胞质嗜酸性,并伴有局灶性腺体成分。通过使用免疫组化染色进行回顾性分析,在切除的 GC 和转移性肝癌中,Glypican 3 呈部分阳性,spalt 样转录因子 4(SALL-4)呈强阳性,表明 GAED 转移到了肝脏。 虽然 GAED 极其罕见,但外科医生应将其视为 GC 的特殊类型之一。GAED 的治疗指南尚未制定;但是,当遇到 APGC 时,通过 Glypican 3 和 SALL-4 的免疫组化染色对 GAED 进行病理确认对于识别其不同于传统 GC 的恶性生物学行为至关重要。
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