胃原发性癌肉瘤4例临床病理分析并文献复习OA
Primary gastric carcinosarcoma:Clinicopathological analysis of 4 cases and literature review
目的:癌肉瘤是指同时具有癌成分和肉瘤成分的恶性肿瘤,恶性程度高,原发胃的癌肉瘤罕见.本文通过探究胃原发性癌肉瘤的临床病理学特征,旨在提高对该肿瘤的认识.方法:回顾性分析苏州大学附属第一医院2017年1月至2023年1月期间收治的胃原发性癌肉瘤4例,并结合相关文献对其临床病理特征、免疫组织化学结果及预后进行总结分析.结果:4例患者中,男3例,女1例.平均年龄为69.8岁.3例因腹痛就诊,1例因持续黑便就诊.肿瘤位于贲门1例,胃底1例,胃窦2例.大体上,肿块呈隆起型,2例为Borrmann I型,2例伴有坏死、为Borrmann Ⅱ型,平均最大直径为7.1 cm.镜下肿瘤均由明确的癌及肉瘤2种成分组成:癌成分的类型主要有管状腺癌、乳头状腺癌、肝样腺癌及鳞状细胞癌;肉瘤成分有横纹肌肉瘤、梭形细胞未分化肉瘤及多形性未分化肉瘤.2种成分所占比例的差异较大,肉瘤成分占比 10%~95%不等.免疫组织化学结果显示癌成分表达细胞角蛋白(cytokeratin,CK)(AE1/AE3),肉瘤成分表达波形蛋白,管状腺癌和乳头状腺癌表达CK7和CK18,鳞状细胞癌表达CK5/6、蛋白(protein,P)63和P40,肝样腺癌表达甲胎蛋白和磷酯酰肌醇蛋白聚糖3(glypican-3).随访1~36个月,1例术后辅助放射治疗和化学治疗,3例未进行放射治疗和化学治疗,2例分别于术后2、36个月死亡,其余2例生存.结论:胃原发性癌肉瘤罕见,恶性程度高.HE形态结合免疫组织化学可有助于该肿瘤的诊断与鉴别诊断.
Objective:Carcinosarcoma refers to malignant tumors containing both carcinoma and sarcoma components,with high malignancy.Primary gastric carcinosarcoma is rare.This study aims to investigate the clinicopathological features of primary gastric carcinosarcoma to improve the understanding of this tumor. Methods:Four cases of primary gastric carcinosarcoma admitted to the First Affiliated Hospital of Soochow University from January 2017 to January 2023 were retrospectively analyzed.Their clinicopathological features,immunohistochemical results,and prognosis in conjunction with literature were summarized and analyzed. Results:Among the four cases,there were three males and one female,with a mean age of 69.8 years.Three cases presented with abdominal pain,and one case presented with persistent black stool.The tumors were located in the cardia in one case,the fundus in one case,and the antrum in two cases.Macroscopically,the tumors were protruding masses,with two cases classified as Borrmann type I,and two cases showing necrosis,classified as Borrmann type Ⅱ,with an average maximum diameter of 7.1 cm.Microscopically,the tumors consisted of carcinoma and sarcoma components.The carcinoma components included tubular adenocarcinoma,papillary adenocarcinoma,hepatoid adenocarcinoma,and squamous cell carcinoma.The sarcomatous components included rhabdomyosarcoma,spindle cell undifferentiated sarcoma,and pleomorphic undifferentiated sarcoma.There was significant variability in the proportion of the two components,with sarcoma components ranging from 10%to 95%.Immunohistochemical results showed cytokeratin(CK)(AE1/AE3)expression in carcinoma components and vimentin expression in sarcoma components.Tubular and papillary adenocarcinomas expressed CK7 and CK18.Squamous cell carcinoma expressed CK5/6,protein(P)63,and P40.Hepatoid adenocarcinoma expressed alpha-fetoprotein and proteoglycan 3(glypican-3).During a follow-up period of 1 to 36 months,one case received adjuvant radiotherapy and chemotherapy after surgery,three cases did not receive radiotherapy and chemotherapy,two cases died at 2 and 36 months after surgery,respectively,and the remaining two cases survived. Conclusion:Primary gastric carcinosarcoma is rare and highly malignant.Combined HE morphology and immunohistochemistry can aid in the diagnosis and differential diagnosis of this tumor.
杜明占;祁昌
苏州大学附属第一医院病理科,江苏 苏州 215006
胃肿瘤癌肉瘤临床病理免疫组织化学
gastric tumorcarcinosarcomaclinicopathologyimmunohistochemistry
《临床与病理杂志》 2024 (001)
124-129 / 6
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