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[具有成肌母细胞分化的直肠腺癌的临床病理特征]

[Clinicopathological features of rectal adenocarcinoma with enteroblastic differentiation].

作者信息

Liu J, Liu X L, Lin D L, Zhao H, Li Y J, Xing X M

机构信息

Department of Gastroenterology, Yantai Yeda Hospital, Shandong Province, Yantai 264006, China.

Department of Pathology, the Affiliated Hospital of Qingdao University, Qingdao 266000, China.

出版信息

Zhonghua Bing Li Xue Za Zhi. 2023 Aug 8;52(8):797-801. doi: 10.3760/cma.j.cn112151-20230203-00091.

Abstract

To investigate the clinicopathological features, immunophenotype, and genetic alterations of rectal adenocarcinoma with enteroblastic differentiation. Four cases of rectal adenocarcinoma with enteroblastic differentiation were collected at the Affiliated Hospital of Qingdao University, Qingdao, China (three cases) and Yantai Yeda Hospital of Shandong Province, China (one case) from January to December 2022. Their clinical features were summarized. Hematoxylin and eosin stain and immunohistochemical stain were performed, while next-generation sequencing was performed to reveal the genetic alterations of these cases. All four patients were male with a median age of 65.5 years. The clinical manifestations were changes of stool characteristics, bloody stools and weight loss. All cases showed mixed morphology composed of conventional adenocarcinoma and adenocarcinoma with enteroblastic differentiation. Most of the tumors consisted of glands with tubular and cribriform features. In one case, almost all tumor cells were arranged in papillary structures. The tumor cells with enteroblastic differentiation were columnar, with relatively distinct cell boundaries and characteristic abundant clear cytoplasm, forming fetal gut-like glands. Immunohistochemically, the tumor cells were positive for SALL4 (4/4), Glypican-3 (3/4) and AFP (1/4, focally positive), while p53 stain showed mutated type in 2 cases. The next-generation sequencing revealed that 2 cases had TP53 gene mutation and 1 case had KRAS gene mutation. Rectal adenocarcinoma with enteroblastic differentiation is rare. It shows embryonal differentiation in morphology and immunohistochemistry, and should be distinguished from conventional colorectal adenocarcinoma.

摘要

探讨具有成胚细胞分化的直肠腺癌的临床病理特征、免疫表型及基因改变。2022年1月至12月,在中国青岛大学附属医院(3例)和中国山东省烟台业达医院(1例)收集了4例具有成胚细胞分化的直肠腺癌病例。总结其临床特征。进行苏木精-伊红染色和免疫组织化学染色,同时进行二代测序以揭示这些病例的基因改变。所有4例患者均为男性,中位年龄为65.5岁。临床表现为大便性状改变、便血和体重减轻。所有病例均表现为传统腺癌和成胚细胞分化腺癌的混合形态。大多数肿瘤由具有管状和筛状特征的腺体组成。在1例中,几乎所有肿瘤细胞呈乳头状结构排列。具有成胚细胞分化的肿瘤细胞呈柱状,细胞边界相对清晰,具有特征性丰富的透明细胞质,形成胎儿肠道样腺体。免疫组织化学检查显示,肿瘤细胞SALL4阳性(4/4)、磷脂酰肌醇蛋白聚糖-3阳性(3/4)、甲胎蛋白阳性(1/4,局灶阳性),而p53染色显示2例为突变型。二代测序显示2例有TP53基因突变,1例有KRAS基因突变。具有成胚细胞分化的直肠腺癌罕见。其在形态学和免疫组织化学上表现为胚胎分化,应与传统结直肠癌相鉴别。

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