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Double Pathology: Malignant Epithelial Ovarian Tumor and Germ Cell Tumor (Choriocarcinoma) a Rare Coexistence

机译:双重病理:恶性上皮性卵巢肿瘤和生殖细胞肿瘤(癌)罕见并存

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摘要

Surface epithelial stromal tumors account for approximately 60% of all ovarian tumors and approximately 90% of all ovarian malignancies. Sex cord stromal tumors account for 7% of all malignant ovarian tumors. Germ cell tumors make up only 3-7% of malignant ovarian tumors. A combination of serous carcinoma of the ovary and choriocarcinoma is rare. Until today such combination has been documented only in six cases in the English literature. Here, we describe a case of ovarian serous carcinoma, where histopathology revealed a combination of serous carcinoma with adjacent choriocarcinoma component in the extraovarian peritoneal deposits. A 64-year-old post-menopausal female was diagnosed to have stage IV ovarian cancer. She received six cycles chemotherapy. Subsequently she underwent optimal cytoreductive surgery. Microscopically, monomorphic histology (serous carcinoma) was noted in both the ovaries and dimorphic histologies (serous carcinoma and choriocarcinoma) in the sigmoid mesocolon nodule, omentum and left subdiaphragmatic nodules. Metronomic chemotherapy continued and patient is on regular follow-up for the past 1 year with stable disease. Recognition of choriocarcinomatous components in ovarian carcinomas is important because of its association with aggressive behavior. In spite of the aggressive histology, the patient is surviving for the past 1 year. Different chemotherapeutic regimens have been used in cases of mixed choriocarcinoma and carcinoma, but established chemotherapeutic regimens have not been described. Chemotherapeutic regimens that target both components have been advocated and used. The absence of choriocarcinoma in ovarian primary and its presence in the extraovarian peritoneal deposits have not been described in the English literature so far. This case is being presented for its rarity.
机译:表面上皮间质瘤约占所有卵巢肿瘤的60%,约占所有卵巢恶性肿瘤的90%。性索间质肿瘤占所有恶性卵巢肿瘤的7%。生殖细胞肿瘤仅占卵巢恶性肿瘤的3-7%。卵巢浆液性癌和绒毛膜癌的组合很少见。直到今天,这种组合在英国文献中仅记录在六例中。在这里,我们描述了一个卵巢浆液性癌的病例,其中组织病理学表明浆液性癌与卵巢外腹膜沉积物中相邻的绒毛膜癌成分相结合。一名64岁的绝经后女性被诊断患有IV期卵巢癌。她接受了六个周期的化疗。随后,她接受了最佳的细胞减灭术。在显微镜下,乙状结肠中结肠结节,大网膜和左dia下结节在卵巢和双态组织学(浆液性癌和绒毛膜癌)中均表现为单形组织学(浆液性癌)。继续进行节律性化学疗法,并且在过去1年中对病情稳定的患者进行定期随访。卵巢癌中绒毛膜癌成分的识别很重要,因为它与攻击行为有关。尽管组织学表现出侵略性,但患者仍存活了过去的1年。在混合绒毛膜癌和癌的病例中已经使用了不同的化疗方案,但是尚未描述已建立的化疗方案。已经提倡并使用了靶向两种成分的化学治疗方案。迄今为止,英语文献中没有描述卵巢原发性绒毛膜癌的存在及其在卵巢外腹膜沉积物中的存在。此案例因其稀有性而被提出。

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