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胃胚细胞瘤模拟前肠的胚胎间叶组织:病例报告。

Gastroblastoma mimics the embryonic mesenchyme of the foregut: a case report.

机构信息

Department of Molecular Diagnostic Pathology, School of Medicine, Iwate Medical University, 2-1-1 Idaitoiri, Yahaba, Shiwa, Iwate, Japan.

Department of Surgery, School of Medicine, Iwate Medical University, Shiwa, Japan.

出版信息

Diagn Pathol. 2023 Feb 17;18(1):24. doi: 10.1186/s13000-023-01310-2.

Abstract

BACKGROUND

Gastroblastoma is a rare gastric tumor composed of epithelial and spindle cell components. The characteristic MALAT-GLI1 fusion gene has only been identified in 5 reported cases. We report the morphological characterization of gastroblastoma with the MALAT1-GLI1 fusion gene in a young Japanese woman.

CASE PRESENTATION

A 29-year-old Japanese woman visited Iwate Medical University Hospital with upper abdominal pain. Computed tomography revealed a tumor in expansive lesions involving the gastric antrum. Histologically, we observed a biphasic morphology composed of epithelial and spindle cell components. The epithelial components appeared as slit-like glandular structures with tubular or rosette-like differentiation. The spindle cell components consisted of short spindle-shaped oval cells. Immunohistochemical (IHC) analysis revealed that the spindle cell component was positive for vimentin, CD10, CD56, GLI1, and HDAC2, and focally positive for PD-L1. The epithelial component was positive for CK AE1/AE3, CAM5.2, and CK7, and negative for CK20 and EMA. Both components were negative for KIT, CD34, DOG1, SMA, desmin, S100 protein, chromogranin A, synaptophysin, CDX2, and SS18-SSX. The MALAT-GLI1 fusion gene was detected molecularly.

CONCLUSIONS

We report the following new findings with this case: (i) gastric tumors mimic the gastrointestinal mesenchyme in the embryonic period; (ii) nuclear expression of PD-L1 and HDAC2 were observed in the spindle cell component of a gastroblastoma. We speculate that histone deacetylase (HDAC) inhibitors may offer a promising treatment option for gastroblastoma.

摘要

背景

胃母细胞瘤是一种罕见的胃肿瘤,由上皮细胞和梭形细胞成分组成。特征性的 MALAT-GLI1 融合基因仅在 5 例报道中被发现。我们报告了一例年轻日本女性胃母细胞瘤的形态学特征,并伴有 MALAT1-GLI1 融合基因。

病例介绍

一位 29 岁的日本女性因上腹痛就诊于岩手医科大学医院。计算机断层扫描显示胃窦部有一个膨胀性病变的肿瘤。组织学上,我们观察到一种由上皮细胞和梭形细胞成分组成的双相形态。上皮成分表现为具有管状或玫瑰花结样分化的缝隙状腺管状结构。梭形细胞成分由短梭形卵圆形细胞组成。免疫组织化学(IHC)分析显示,梭形细胞成分阳性表达 vimentin、CD10、CD56、GLI1 和 HDAC2,局部阳性表达 PD-L1。上皮成分阳性表达 CK AE1/AE3、CAM5.2 和 CK7,阴性表达 CK20 和 EMA。两种成分均阴性表达 KIT、CD34、DOG1、SMA、结蛋白、S100 蛋白、嗜铬粒素 A、突触素、CDX2 和 SS18-SSX。分子上检测到 MALAT-GLI1 融合基因。

结论

我们报告了这个病例的以下新发现:(i)胃肿瘤在胚胎期模拟胃肠道间质;(ii)胃母细胞瘤梭形细胞成分中观察到 PD-L1 和 HDAC2 的核表达。我们推测组蛋白去乙酰化酶(HDAC)抑制剂可能为胃母细胞瘤提供一种有前途的治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42d6/9936656/bf12e94ad8ee/13000_2023_1310_Fig1_HTML.jpg

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