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胃SWI/SNF复合体缺失的产甲胎蛋白腺癌临床病理学特征

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目的 探讨胃SWI/SNF复合体缺失的产甲胎蛋白腺癌的临床病理学特征.方法 收集复旦大学附属中山医院2021年1月至2022年12月确诊的胃SWI/SNF复合体缺失的产甲胎蛋白腺癌4例,复习其组织形态学特征、免疫组织化学、EB病毒编码的RNA(EBER)原位杂交、二代测序结果及临床治疗经过,总结其临床病理特征及治疗,并进行文献复习.结果 4例患者中男性3例,女性1例,临床主诉腹痛、嗳气和黑便,其中3例血清甲胎蛋白显著升高,内镜均显示溃疡型病变.镜下观察肿瘤细胞呈弥漫性片状或巢状生长,表现为典型肝样腺癌特征;2例部分区域呈腺样生长,腺样区域胞质透亮,表现为肠母细胞分化.肿瘤细胞核显著异型,可见显著大核仁,核分裂象易见.免疫组织化学结果显示肝样腺癌标志物甲胎蛋白、GPC3和SALL4均阳性,广谱细胞角蛋白和E-cadherin均未见缺失表达.SWI/SNF复合体亚基表达蛋白免疫组织化学检测,即INI1(SMARCB1)、BRG1(SMARCA4)、BRM(SMARCA2)、ARID1A蛋白,4例肝样腺癌区域及肠母细胞分化区域均为SMARCA2缺失表达,其中1例肠母细胞分化区域合并ARID 1A缺失,未见SMARCB1、SMARCA4缺失.4例p53蛋白均呈弥漫阳性,Ki-67阳性指数80%~90%.错配修复蛋白检测均无缺失表达,HER2检测仅1例为3+,EBER均阴性.4例病例二代测序均未检测到SWI/SNF复合体相关亚基的突变.4例中2例因手术时存在远处转移,行姑息性手术,另外2例行根治性切除,3例随访患者术后辅助化疗.结论 产甲胎蛋白腺癌是一组少见的胃癌亚型,可合并SWI/SNF复合体缺失,病理形态学表现与经典SWI/SNF复合体缺失的伴有横纹肌样特征的未分化癌不同.
Clinicopathological features of gastric alpha-fetoprotein-producing adenocarcinoma with SWI/SNF complex deletion
Objective To investigate the clinicopathological features and treatment of gastric alpha-fetoprotein(AFP)-producing adenocarcinoma with SWI/SNF complex deletion.Methods Four cases of gastric AFP-producing adenocarcinoma with SWI/SNF complex deletion diagnosed in Zhongshan Hospital of Fudan University from January 2021 to December 2022 were collected,and their histomorphological characteristics,immunohistochemical(IHC),in situ hybridization of Epstein-Barr virus-encoded RNA(EBER),next-generation sequencing results,clinicopathological features and treatment were summarized,and literature review was conducted.Results Among the 4 patients,there were three males and one female.They presented with abdominal pain,belching and melena.Serum AFP was significantly elevated in three patients,and endoscopy showed ulcerative lesions.Microscopically,the tumor cells showed mainly diffuse flaky or nest-like growth and typical characteristics of hepatoid adenocarcinoma.In two cases there were adenoid growth,and the tumor cells in these areas possessed clear cytoplasm,suggesting enteroblastic differentiation.The tumor cell nuclei were pleomorphic with large nucleoli and brisk mitoses.The IHC results showed that the tumor cells expressed AFP,GPC3 and SALL4,and there was retained expression of broad-spectrum keratin(CKpan)and E-cadherin.IHC detection of SWI/SNF complex subunits,namely INI1(SMARCB1),BRG1(SMARCA4),BRM(SMARCA2),ARID1A protein was performed.In all four cases the hepatoid adenocarcinoma region and enteroblastic differentiation region showed SMARCA2 deletion,and one case with enteroblastic differentiation also showed ARID1A deletion.SMARCB1 and SMARCA4 deletions were not seen.All the four cases were diffusely positive for p53 protein,and the Ki-67 proliferation index was 80%-90%.There were no mismatch repair deletion detected;one cases showed HER2 was strongly positive(3+),and EBER was negative.None of the four cases had mutations in the SWI/SNF complex-related subunits detected by next-generation sequencing.Among the four patients,two underwent palliative surgery due to distant metastasis at the time of surgery,two underwent radical resection.Postoperative adjuvant chemotherapy was given to three patients.Conclusions AFP-producing adenocarcinoma is a rare subtype of gastric cancer,which can be combined with SWI/SNF complex deletion,and the pathomorphological manifestations are different from the classical SWI/SNF complex deletion of undifferentiated carcinoma with rhabdoid phenotype.

Stomach neoplasmsAdenocarcinomaalpha-FetoproteinsSWI/SNF complex deletion

杨洁真、郭欣欣、徐晨、侯英勇、袁伟

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复旦大学附属中山医院厦门医院病理科,厦门 361015

复旦大学附属中山医院病理科,上海 200032

胃肿瘤 腺癌 甲胎蛋白类 SWI/SNF复合体缺失

上海市科委科研项目

19MC1911000

2024

中华病理学杂志
中华医学会

中华病理学杂志

CSTPCD北大核心
影响因子:1
ISSN:0529-5807
年,卷(期):2024.53(1)
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