Malignant dysgerminomatous germ cell tumor of ovary

Malignant dysgerminomatous germ cell tumor of ovary is the most common form of malignant germ cell tumor of ovary, arising from germ cells in the ovary, usually presenting during adolescence with pelvic mass, fever, vaginal bleeding, and acute abdomen and is characterized by bilaterality (around 10% of cases), association with dysgenetic gonads (5 to 10% of cases), elevated serum lactate dehydrogenase (LDH) and human chorionic gonadotrophin (hCG) (in the presence of syncitiotrophoblasts). Malignant dysgerminomatous germ cell tumor of ovary responds well to chemotherapy, potentially sparing patients from infertility and early mortality.

Also known as: dysgerminomatous germ cell cancer of ovary, dysgerminomatous germ cell cancer of the ovary, malignant ovarian dysgerminoma, malignant dysgerminomatous germ cell tumor of the ovary, malignant dysgerminomatous germ cell tumour of the ovary

2839 clinical trials for this condition and its sub-types, 0 tagged with Malignant dysgerminomatous germ cell tumor of ovary itself.