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Endometrioid adenocarcinoma with choriocarcinomatous differentiation: A case report and review of the literature

机译:子宫内膜样腺癌与绒毛膜癌的分化:一例报道并文献复习

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A choriocarcinomatous component is rarely present in carcinomas of certain sites and few cases of choriocarcinomatous differentiation in endometrioid adenocarcinoma have been reported. The present study reports a case of endometrioid adenocarcinoma of the uterine corpus with choriocarcinomatous differentiation, and discusses the clinicopathological features of this rare tumor. A 59-year-old post-menopausal female presented with abnormal vaginal bleeding. Magnetic resonance imaging demonstrated a relatively well-circumscribed tumor in the uterine corpus and a total cystectomy was subsequently performed. A histopathological examination revealed two distinct components in the uterine corpus tumor. The first component comprised ~80% of the tumor and was composed of poorly-differentiated endometrioid adenocarcinoma. The remaining component consisted of mononucleated and syncytial giant cells containing rich eosinophilic cytoplasm and large pleomorphic nuclei with coarse chromatin. An immunohistochemical analysis revealed that these syncytial giant cells were positive for β-human chorionic gonadotropin (hCG). Therefore, a diagnosis of endometrioid adenocarcinoma with choriocarcinomatous differentiation was confirmed. The clinicopathological features of nine previously reported cases of this tumor were analyzed in addition to the present case. The majority of the patients were post-menopausal. Endometrial choriocarcinoma may be considered to have a highly aggressive clinical course, since nine of the 10 cases displayed metastases and four patients succumbed to the disease. The pathogenesis of the choriocarcinomatous component is not well understood. However, genetic studies have demonstrated that conventional carcinoma and choriocarcinomatous components share common genetic alterations. The choriocarcinomatous component represents aberrant differentiation of the conventional carcinoma, however, genetic analyses of endometrioid adenocarcinoma with choriocarcinomatous differentiation have not been performed.
机译:在某些部位的癌中很少存在绒毛膜癌成分,并且已经报道了子宫内膜样腺癌中绒毛膜癌分化的病例很少。本研究报告了一例子宫内膜样腺癌伴绒毛膜癌的分化,并讨论了这种罕见肿瘤的临床病理特征。一名59岁的绝经后女性出现异常阴道出血。磁共振成像显示子宫体中肿瘤的界限相对较好,随后进行了全膀胱切除术。组织病理学检查显示子宫体肿瘤中有两个不同的组成部分。第一部分约占肿瘤的80%,由低分化子宫内膜样腺癌组成。其余成分由单核细胞和合胞体巨细胞组成,其中含有丰富的嗜酸性细胞质和大的多形核,并带有粗染色质。免疫组织化学分析显示,这些合胞体巨细胞对β-人绒毛膜促性腺激素(hCG)呈阳性。因此,证实了诊断为子宫内膜样腺癌与绒毛膜癌的分化。除本病例外,还分析了九例先前报道的该肿瘤的临床病理特征。大多数患者是绝经后。子宫内膜绒毛膜癌可被认为具有高度侵袭性的临床病程,因为10例病例中有9例显示有转移,而4例则死于该病。绒毛膜癌成分的发病机理尚不清楚。然而,遗传研究表明,常规癌和绒癌组织具有共同的遗传改变。绒毛膜癌成分代表常规癌的异常分化,但是,尚未进行具有绒毛膜癌分化的子宫内膜样腺癌的遗传分析。

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