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卵巢甲状腺样类癌——两例报告并文献复习

Strumal carcinoid of the ovary - report of two cases and review of literature.

作者信息

Macháleková K, Kolníková G, Redecha M, Žúbor P, Kajo K

出版信息

Ceska Gynekol. 2018 Winter;83(6):452-457.

Abstract

OBJECTIVE

Strumal carcinoid (SC) is a rare ovarian germ-cell tumour, which is characterized by a mixture of thyroid tissue and carcinoid. It can be presented as a monodermal teratoma or as a part of mature cystic teratoma (dermoid cyst).

DESIGN

Case report.

SETTING

Department of pathology, St. Elisabeth Cancer Institute, Bratislava.

METHODS AND RESULTS

Hereby the authors describe two cases of this rare tumour in clinically asymptomatic women, 46- and 52-year-old, whom tumours were diagnosed at preventive gynaecological examination. The tumours considered of solid - cystic features, measured 65×45×40 mm and 75×45×40 mm and both contained parts of SC represented by tougher yellowish gelatinous areas. In both cases, SC was a part of the mature cystic teratoma (dermoid cyst), with predominated content. Histologically, both SC had a characteristic composition of intimate mixture of mature thyroid tissue and carcinoid. Immunohistochemically, the thyroid tissue stained positively with cytokeratin7, thyroglobulin and thyroid transcription factor-1, and the carcinoid component exhibited expression of synaptophysin and chromogranin A (only in one case). Tumour cells of both components of SC were negative for calcitonin and carcinoembryonic antigen. Both tumours showed low proliferation activity expressed by Ki-67 (up to 2%). Tumours were diagnosed in stage IA, and up to now are patients without any complications associated with tumours, free of relapse for 3 years and 6 months, respectively.

CONCLUSION

SC represents an interesting form of primary ovarian carcinoid, which is usually asymptomatic and when confined to ovary, mostly has benign behaviour and can be treated by simple one-sided or bilateral adnexectomy. Keywords ovary, germ cell tumours, strumal carcinoid, immunohistochemistry.

摘要

目的

甲状腺类癌(SC)是一种罕见的卵巢生殖细胞肿瘤,其特征为甲状腺组织和类癌混合存在。它可表现为单胚层畸胎瘤或成熟囊性畸胎瘤(皮样囊肿)的一部分。

设计

病例报告。

单位

布拉迪斯拉发圣伊丽莎白癌症研究所病理科。

方法与结果

作者在此描述两例该罕见肿瘤病例,患者为46岁和52岁临床无症状女性,肿瘤在预防性妇科检查时被诊断。肿瘤具有实性 - 囊性特征,大小分别为65×45×40毫米和75×45×40毫米,两者均包含由较硬的淡黄色胶冻状区域代表的SC部分。两例中,SC均为成熟囊性畸胎瘤(皮样囊肿)的一部分,含量占优势。组织学上,两个SC均具有成熟甲状腺组织和类癌紧密混合的特征性组成。免疫组化方面,甲状腺组织细胞角蛋白7、甲状腺球蛋白和甲状腺转录因子 - 1染色呈阳性,类癌成分显示突触素和嗜铬粒蛋白A表达(仅在一例中)。SC两种成分的肿瘤细胞降钙素和癌胚抗原均为阴性。两个肿瘤Ki - 67表达显示增殖活性低(高达2%)。肿瘤诊断为IA期,截至目前患者无任何与肿瘤相关的并发症,分别无复发3年零6个月。

结论

SC是原发性卵巢类癌的一种有趣形式,通常无症状,局限于卵巢时大多具有良性行为,可通过简单的单侧或双侧附件切除术治疗。关键词:卵巢、生殖细胞肿瘤、甲状腺类癌、免疫组化

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