Diagnostics and treatment of rare ovarian malignancies

被引:0
|
作者
Hetterich, Madeleine [1 ]
Ortmann, Olaf [1 ]
机构
[1] Univ Frauenklin Regensburg, Caritas Krankenhaus St Josef, Landshuter Str 65, D-93053 Regensburg, Germany
来源
GYNAKOLOGIE | 2023年 / 56卷 / 1期
关键词
Gynecological oncology; Germ cell tumors; Non-epithelial ovarian malignancies; Teratoma; Sex cord stromal tumors; GERM-CELL TUMORS; YOLK-SAC TUMORS; COMBINATION CHEMOTHERAPY; PROGNOSTIC IMPACT; MANAGEMENT; BLEOMYCIN; CISPLATIN; SURVIVAL; VINBLASTINE; ETOPOSIDE;
D O I
10.1007/s00129-022-05038-w
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Ovarian cancer is the fifth most frequent cancer in women. The relative 5-year survival is currently 42% [1]. The rarer gynecological neoplasms include nonepithelial ovarian tumors; ovarian sex cord stromal tumors with ca. 8% and malignant germ cell tumors with ca. 3-10% of all primary ovarian tumors make up a large part of this rare group [2, 3]. Other very rare malignant ovarian neoplasms that need to be distinguished are small cell (of the pulmonary or hypercalcemic type) and neuroendocrine ovarian carcinomas, sarcomas and lymphomas. Due to the low incidence of these neoplasms there are only a few evidence-based guidelines as a basis for action. Affected patients should therefore be connected to specialized gynecological oncology centers and the possibility of participating in a study should be examined (for an overview of the current study groups and studies carried out see ). Patient data should be collected in cancer registries.
引用
收藏
页码:28 / 37
页数:10
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